Beximco Pharmaceutical

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First Aid Empty Bag

First Aid Empty Bag

Tk.450.00/=
Trulicity 0.75/0.5ml

Trulicity 0.75/0.5ml

Tk.3,395.00/=
MaxD 40000 IU Capsule
Smile Baby Diaper 5's M
Smile Baby Diaper 5's S
Raja Super Condom
Amore Black Condom

Amore Black Condom

Tk.100.00/=
Amore gold condom

Amore gold condom

Tk.100.00/=
Hero Condom 1 packet
Terbin 15 gm Cream

Terbin 15 gm Cream

Tk.80.00/=
Valmor 100 Tablet

Valmor 100 Tablet

Tk.85.00/=
Tolfem 200 mg Tablet
Enaril 5

Enaril 5

1. What is and what it is used for?Enaril (Enalapril Maleate) is the maleate salt of enalapril, the ethyl ester of a long-acting angiotensin converting enzyme inhibitor, enalaprilat. It is highly effective in the management of hypertension and heart failure. Enaril is available as 5 mg tablet for oral administration. Enaril is indicated for the treatment of all grades of essential hypertension, renovascular hypertension and heart failure.2. Before you take EnarilDo not take this medicine and tell your doctor if:Enalapril is contraindicated in patients who are hypersensitive to any component of this product and in patients with a history of angioneurotic oedema relating to previous treatment with an ACE inhibitor.Do not take this medicine if the above applies to you. If you are not sure, talk to your doctor before taking Dilapress.Take special care with EnarilHypotension: Symptomatic hypotension has been reported mainly in patients with severe heart failure. In these patients, by discontinuing diuretic therapy or significantly reducing the diuretic dose for two to three days prior to initiating Enalapril, the possibility of this occurrence is reduced. By initiating therapy with a small dose (2.5 mg), the duration of any hypotensive effect may be lessened.If hypotension develops, the patient should be placed in a supine position. Volume repletion with oral fluids or intravenous normal saline may be required.Impaired renal function: Enalapril should be used with caution in patients with renal insufficiency as they may require reduced or less frequent doses. Renal failure has been reported in association with Enalapril and has been mainly in patients with severe congestive heart failure or underlying renal disease, including renal artery stenosis. If recognized promptly and treated appropriately, renal failure is usually reversible.Cough: Cough has been reported with the use of ACE inhibitors.Surgery/Anesthesia: In patients undergoing major surgery or during anesthesia with agents that produce hypotension, Enalapril blocks angiotensin II formation secondary to compensatory renin release.This may lead to hypotension which can be corrected by volume expansion.Taking other medicinesCombination with other antihypertensive agents such as beta-blockers, methyldopa, calcium antagonists and diuretics may increase the antihypertensive efficacy. Adrenergic-blocking drugs should only be combined with Enalapril under careful supervision. Concomitant propranolol may reduce the bioavailability of Enalapril, but this does not appear to be of any clinical significance. Concomitant therapy with lithium may increase the serum lithium concentration.Pregnancy and breast-feedingEnalapril is contraindicated in pregnancy and treatment should be stopped if pregnancy is suspected, because it has been shown to be foetotoxic in rabbits. : Enalapril and Enalaprilat are excreted in breast milk ; caution should be exercised if Enalapril is given to lactating mothers.3. How to take Enaril?Essential and Renovascular Hypertension : Treatment should be initiated with 5 mg once a day. Where concomitant therapy is a diuretic, the recommended initial dose of Enaril is 2.5 mg. The dose should be titrated to give optimum control of blood pressure. The usual maintenance dose is 10-20 mg given once daily. In severe hypertension, the dosage may be increased incrementally to a maximum of 40 mg once daily.Heart failure : Enaril can be used as an adjunctive therapy with non-potassium-sparing diuretics and / or digitalis. The recommended starting dose of Enaril is 2.5 mg once daily. The dose of Enaril should be gradually increased depending upon tolerability to the recommended maintenance dose (10-20 mg) given as a single or twice daily dose.If you take more Enaril than you shouldLimited data are available for overdosage in humans. The most prominent feature of overdosage is hypotension, for which the usual treatment would be intravenous infusion of normal saline solution. Enalapril can be removed from the general circulation by haemodialysis.If you forget to take EnarilIf you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten dose.If you stop taking EnarilDo not stop taking this medicine without talking to your doctor. You should not stop taking Enaril just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsLike all medicines, Enaril can cause side effects, although not everybody gets them.The commonly reported side effects are dizziness and headache. Other side effects occurring less frequently include orthostatic hypotension, nausea, rash, cough etc.Cardiovascular: Myocardial infarction or cerebrovascular accident, possibly secondary to severe hypotension in high-risk patient..

Tk.1.00/=

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Enegra 100 tablet

Enegra 100 tablet

Enegra 100 tablet1. What Enegra® is and what it is used for?Sildenafil Citrate, is the citrate salt of sildenafil, a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type-5 (PDE5). It is used for Erectile dysfunction and Pulmonary hypertension.2. Before you take Enegra®Caution is advised when phosphodiesterase type 5 (PDE5) inhibitors are co-administered with alpha-blockers. PDE5 inhibitors, including sildenafil, and alpha-adrenergic blocking agents are both vasodilators with blood pressure lowering effects. When vasodilators are used in combination, an additive effect on blood pressure may be anticipated. In some patients, concomitant use of these two drug classes can lower blood pressure significantly, leading to symptomatic hypotension. In the sildenafil interaction studies with alpha-blockers, cases of symptomatic hypotension consisting of dizziness and lightheadedness were reported. No cases of syncope or fainting were reported during these interaction studies. Sildenafil Citrate should be used with caution in patients with anatomical deformation of the penis (such as angulation, cavernosal fibrosis or Peyronie’s disease) or in patients who have conditions, which may predispose them to priapism (such as sickle cell anemia, multiple myeloma or leukemia).3. How to take Enegra®How much to takeErectile dysfunction: For most patients, the recommended dose is 50 mg taken, as needed, approximately 1 hour before sexual activity. However, Enegra® may be taken anywhere from 4 hours to 0.5 hour before sexual activity. Based on effectiveness and toleration, the dose may be increased to a maximum recommended dose of 100 mg or decreased to 25 mg. The maximum recommended dosing frequency is once per day. Pulmonary hypertension: 20 mg 3 times daily.If you forget to take Enegra®If you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten doseIf you stop taking Enegra®Do not stop taking this medicine without talking to your doctor. You should not stop taking Enegra® just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsThe most common side effects are headache, flushing of the face, and upset stomach. Less common side effects that may occur are temporary changes in color vision, eyes being more sensitive to light, or blurred vision.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet.5. How to store Enegra®?Keep in a cool & dry place, protected from light. Keep out of the reach of children...

Tk.50.00/=

  0 отзывов

Enegra 50 tablet

Enegra 50 tablet

Enegra 50 tablet1. What Enegra® is and what it is used for?Sildenafil Citrate, is the citrate salt of sildenafil, a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type-5 (PDE5). It is used for Erectile dysfunction and Pulmonary hypertension.2. Before you take Enegra®Caution is advised when phosphodiesterase type 5 (PDE5) inhibitors are co-administered with alpha-blockers. PDE5 inhibitors, including sildenafil, and alpha-adrenergic blocking agents are both vasodilators with blood pressure lowering effects. When vasodilators are used in combination, an additive effect on blood pressure may be anticipated. In some patients, concomitant use of these two drug classes can lower blood pressure significantly, leading to symptomatic hypotension. In the sildenafil interaction studies with alpha-blockers, cases of symptomatic hypotension consisting of dizziness and lightheadedness were reported. No cases of syncope or fainting were reported during these interaction studies. Sildenafil Citrate should be used with caution in patients with anatomical deformation of the penis (such as angulation, cavernosal fibrosis or Peyronie’s disease) or in patients who have conditions, which may predispose them to priapism (such as sickle cell anemia, multiple myeloma or leukemia).3. How to take Enegra®How much to takeErectile dysfunction: For most patients, the recommended dose is 50 mg taken, as needed, approximately 1 hour before sexual activity. However, Enegra® may be taken anywhere from 4 hours to 0.5 hour before sexual activity. Based on effectiveness and toleration, the dose may be increased to a maximum recommended dose of 100 mg or decreased to 25 mg. The maximum recommended dosing frequency is once per day. Pulmonary hypertension: 20 mg 3 times daily.If you forget to take Enegra®If you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten doseIf you stop taking Enegra®Do not stop taking this medicine without talking to your doctor. You should not stop taking Enegra® just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsThe most common side effects are headache, flushing of the face, and upset stomach. Less common side effects that may occur are temporary changes in color vision, eyes being more sensitive to light, or blurred vision.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet.5. How to store Enegra®?Keep in a cool & dry place, protected from light. Keep out of the reach of children...

Tk.30.00/=

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Epilep 200

Epilep 200

Epilep® contains Carbamazepine which is an iminodibenzyl derivative with anticonvulsant properties and its structure is related to the tricyclic antidepressants. Carbmazepine is indicated in all forms of epilepsy except myoclonic and absence seizures. It is also indicated in trigeminal neuralgia, mood disorder, aggreession and diabetes insipidus...

Tk.3.51/=

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Epilep CR

Epilep CR

Epilep CREpilep® contains Carbamazepine which is an iminodibenzyl derivative with anticonvulsant properties and its structure is related to the tricyclic antidepressants. Carbmazepine is indicated in all forms of epilepsy except myoclonic and absence seizures. It is also indicated in trigeminal neuralgia, mood disorder, aggreession and diabetes insipidus...

Tk.4.52/=

  0 отзывов

Exovate Cream

Exovate Cream

Clobetasol Propionate is a very active topical corticosteroid which is of particular value when used in short courses for the treatment of more resistant dermatoses such as psoriasis (excluding widespread plaque psoriasis), recalcitrant eczemas and other conditions which do not respond satisfactorily to less active steroids.A small quantity should be applied to the affected area once or twice daily until improvement occurs. Therapy should be discontinued when control is achieved. It is recommended that treatment should not be continued for more than two or four weeks without the patients’ condition being reviewed.Highly potent than other corticosteroidsProvides confidence in treating all moderate to severe dermatosesEnsures better treatment in all types of skin infections..

Tk.45.00/=

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Exovate N cream

Exovate N cream

Clobetasol Propionate is a highly active corticosteroid with topical anti-inflammatory activity. The major effect of Clobetasol Propionate on skin is a non-specific antiinflammatory response, partially due to vasoconstriction and decrease in collagen synthesis. The use of Nystatin in the local treatment of candidal infections of the skin and of Neomycin as a broad-spectrum antibiotic is well known.Exovate® N cream is indicated in more resistant dermatoses such as recalcitrant eczemas and psoriasis (excluding widespread plaque psoriasis) where secondary bacterial or candidal infection is present, suspected or likely to occur, as when using occlusive dressings.Effective against non-responsive dermatosesEffective against allergic and pruritic conditionsEffective against bacterial and fungal skin infections..

Tk.90.00/=

  0 отзывов

Exovate N Ointment

Exovate N Ointment

Exovate N OintmentClobetasol Propionate is a highly active corticosteroid with topical anti-inflammatory activity. The major effect of Clobetasol Propionate on skin is a non-specific antiinflammatory response, partially due to vasoconstriction and decrease in collagen synthesis. The use of Nystatin in the local treatment of candidal infections of the skin and of Neomycin as a broad-spectrum antibiotic is well known.Exovate® N cream is indicated in more resistant dermatoses such as recalcitrant eczemas and psoriasis (excluding widespread plaque psoriasis) where secondary bacterial or candidal infection is present, suspected or likely to occur, as when using occlusive dressings.Effective against non-responsive dermatosesEffective against allergic and pruritic conditionsEffective against bacterial and fungal skin infections..

Tk.100.00/=

  0 отзывов

Exovate Ointment

Exovate Ointment

Exovate OintmentClobetasol Propionate is a very active topical corticosteroid which is of particular value when used in short courses for the treatment of more resistant dermatoses such as psoriasis (excluding widespread plaque psoriasis), recalcitrant eczemas and other conditions which do not respond satisfactorily to less active steroids.A small quantity should be applied to the affected area once or twice daily until improvement occurs. Therapy should be discontinued when control is achieved. It is recommended that treatment should not be continued for more than two or four weeks without the patients’ condition being reviewed.Highly potent than other corticosteroidsProvides confidence in treating all moderate to severe dermatosesEnsures better treatment in all types of skin infections..

Tk.50.00/=

  0 отзывов

Fertil 50 mg Tab

Fertil 50 mg Tab

Fertil 50 mg TabFertil® is an ovulatory stimulant which is indicated for the treatment of ovulatory dysfunction in women desiring pregnancy. Clomiphene citrate is indicated for the treatment of ovulatory failure in women desiring pregnancy whose partners are fertile and potent.Fertil is an ovulatory stimulant which is indicated for the treatment of ovulatory dysfunction in women desiring pregnancy.Clomiphene citrate is indicated for the treatment of ovulatory failure in women desiring pregnancy whose partners are fertile and potent...

Tk.10.00/=

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Fibropress 10 tab

Fibropress 10 tab

1. What Fibropress® is and what it is used for?Uterine fibroids are a major cause of morbidity in women of a reproductive age. The management of symptomatic fibroids has traditionally been surgical. However, USFDA recently approved ulipristal acetate, an oral selective progesterone-receptor modulator, for the same indication. Ulipristal acetate is a new, effective, and well-tolerated option for the preoperative treatment of moderate and severe symptoms of uterine fibroids in women of reproductive age. Clinical data shows ulipristal acetate has several advantages: it acts faster in reducing the fibroid-associated bleeding, it significantly improves hemoglobin and hematocrit levels in anemic patients, and it grants a significant reduction in the size of fibroids.Uses:Ulipristal acetate is indicated for pre-operative treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.2. How to take this medicine?The treatment consists of one tablet of 5 mg to be taken once daily for treatment courses of up to 3 months each. Tablets may be taken with or without food3. Who should NOT take this medication?Fibropress is contraindicated in:Contact your doctor if you experience these side effects and they are severe or bothersome.Hypersensitivity to the drug or to any of its components.Pregnancy and breastfeeding.Genital bleeding of unknown aetiology or for reasons other than uterine fibroids.Uterine, cervical, ovarian or breast cancer.4. What special precautions for use?Ulipristal acetate should only be prescribed after careful diagnosis. Pregnancy should be precluded prior to treatment. If pregnancy is suspected prior to initiation of a new treatment course, a pregnancy test should be performed. Other precautions include;Patients with severe renal or moderate to severe hepatic impairment.Women with Endometrial changes, reduction in menstrual blood loss or amenorrhea.Not recommended w/ concomitant use of progestagen-only pills, a progestagen-releasing IUD or combined OC pills.5. What side effects are possible with this medication?Amenorrhea, hot flush, endometrial thickening. Headache; vertigo; abdominal pain, nausea; acne, hyperhidrosis; musculoskeletal pain; uterine hemorrhage, pelvic pain, ovarian cyst, breast tenderness/pain; edema, fatigue; increased blood cholesterol.6. How supplied and storage condition of Fibropress® Tablet?Fibropress® Tablet: Box containing 10 tablets in 1X10’s blister strip. Each tablet contains Ulipristal acetate INN 5 mg.Fibropress®must be kept out of the reach and sight of children. Protect from light and store below 30°C...

Tk.55.00/=

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Filmet 400 tablet

Filmet 400 tablet

Filmet 400 tablet1. What Filmet is and what it is used for?Filmet is a sterile, pyrogen free, isotonic formulation for intravenous administration in susceptible life threatening infections. Each 100ml solution contains Metronidazole USP 500mg. Metronidazole is a nitroimidazole with antiprotozoal and antibacterial actions. It is highly effective against Trichomonas vaginalis, Entamoeba histolytica and Giardia lamblia. It has a bactericidal action against a wide range of pathogenic anaerobic microorganisms particularly species of Bacteroides, Fusobacteria, Clostridia, Eubacteria, Anaerobic Cocci and Gardnerella vaginalis2. Before you take FilmetDo not take this medicine and tell your doctor if:Known hypersensitivity to metronidazole.Take special care with FilmetCheck with your doctor before taking this medicine if:Regular clinical and laboratory monitoring are advised if administration of Filmet for more than 10 days is considered to be necessary. Metronidazole should be administered with caution to patients with hepatic encephalopathy. Caution is advised in patients with active disease of the central nervous system other than brain abscess. The consumption of alcohol during metronidazole therapy should be avoided since there could be a disulfiram-like reactionPregnancy and breast-feedingThere is inadequate evidence of the safety of metronidazole in pregnancy. Metronidazole is excreted in milk and no adverse effects in the newborn have been reported. Filmet should therefore be given during pregnancy or during lactation only when the physicians consider it essential.3. How to take FilmetAlways use Filmet exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.How much to take?Filmet may be diluted with appropriate volumes of normal saline, dextrose-saline, dextrose 5% w/v or potassium chloride (20 and 40 mmol) infusions.For prophylaxis and treatment of anaerobic infections:Adults: 100 ml (500 mg) immediately before, during or after operation,repeated 8 hourlyChildren: 1.5 ml (7.5 mg) per kg body weight every 8 hoursDuration: Treatment for 7 days should be satisfactory for most patients but depending on clinical and bacteriological assessments, the physician may decide to prolong the treatmentInfusion rate: Filmet should be infused at an approximate rate of 5 ml/minuteIf you take more Filmet than you shouldIf you have too much of this medicine, talk to your doctor straight away.If you forget to take FilmetIf you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten doseIf you stop taking FilmetDo not stop taking this medicine without talking to your doctor. You should not stop taking Filmet just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsLike all medicines, Filmet can cause side effects, although not everybody gets them.Serious adverse reactions occur very rarely with standard recommended regimens. Unpleasant taste in the mouth, furred tongue, nausea, vomiting or other gastrointestinal disturbances have been reported. Urticaria, skin rash, pruritus, angioedema and rarely anaphylaxis have occurred. Drowsiness, dizziness, headache, ataxia and darkening of the urine (due to metabolites) have been reported rarely. Peripheral neuropathy and/or transient epileptiform seizures have occurred during prolonged or intensive treatment but in most cases neuropathy disappears on cessation of therapy. A moderate, reversible leucopenia has been reported in some patientsTell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet5. How to store Filmet?Store in a cool and dry place, away from light. Keep out of reach of children...

Tk.1.70/=

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Filmet 500 mg IV Infusion

Filmet 500 mg IV Infusion

Filmet 500 mgFilmet® IV infusion is a sterile, pyrogen free, isotonic formulation for intravenous administration in susceptible life threatening infections. Metronidazole is a nitroimidazole with antiprotozoal and antibacterial actions. It has bactericidal action against a wide range of pathogenic anaerobic microorganisms. Filmet® IV is indicated in the prevention of post operative infections due to anaerobic bacteria, in the treatment of intraabdomianl infections, gynaecologial and obstetrical infections, respiratory infections etc.Reduces hospital stay timeLessens chance of nosocomial infectionsOffers safety and convenience to patients..

Tk.53.86/=

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Filmet DS Tablet

Filmet DS Tablet

Filmet DS 800..

Tk.2.01/=

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Fixolin 400mg Tab

Fixolin 400mg Tab

Fixolin 400mg TabFixolin® (Doxofylline) is a type of enzyme inhibitor drug that is used to treat Asthma and COPD.Fixolin® (Doxofylline) is a new generation long acting oral methylxanthine derivative.Methylxanthines are phosphodiesterase inhibitors. Fixolin® (Doxofylline) is indicated for maintenance therapy in patients suffering with Asthma and Chronic Obstructive Pulmonary Disease (COPD).Fixolin® (Doxofylline) offers,In COPD, effectively reduces exacerbationsIn asthma, provides better symptom controlNo effect on sleep pattern and awakeningsSafe for cardiac patientsLesser effect on gastric secretionBetter patient compliance..

Tk.5.00/=

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Flatameal DS susp.

Flatameal DS susp.

Flatameal DS susp.Flatameal® DS is an antacid and antiflatulent containing a combination of Aluminium Hydroxide Gel USP, Magnesium Hydroxide BP and Simethicone USP. It is indicated for dyspepsia, hyperacidity, gastric and duodenal ulcer, gastritis also for the relief of flatulence, abdominal distention and windy colic.A unique combination of acid neutralizer + antiflatulentProvides quick & prolonged acid neutralizationEffectively relieves gaseous distressOffers safety to patientsEnsures excellent patients' acceptability..

Tk.75.00/=

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Furasep

Furasep

Furasep 20 gm CreamIndicationsNitrofurazone is indicated in the infectious conditions of the skin such as burns, wounds, ulcers, skin infections and skin grafting.Therapeutic ClassTopical Antibiotic preparationsPharmacologyNitrofurazone is a broad spectrum topical antibacterial agent indicated for the treatment of mixed skin infections of superficial wounds and diseases of the skin.Dosage & AdministrationTo be applied directly to the lesion or on gauze first; 2-3 times daily or as advised by the physician.ContraindicationsNitrofurazone is contraindicated to patients with known sensitivity to Nitrofurazone. It is not advisable to use Nitrofurazone after the infection is cured. It should be used with caution in patients with known or suspected renal impairment.Side EffectsSensitization and generalized allergic skin reactions may be produced after few days of initial application. Cross sensitization to other Nitrofurazone derivatives may occur. Intolerance to Nitrofurazone necessitating withdrawal has been encountered...

Tk.17.00/=

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Gastalfet 500 mg tablet

Gastalfet 500 mg tablet

Gastalfet 500 mg tablet1. What Gastalfet is and what it is used for?Gastalfet tablet contains 500 mg of Sucralfate (basic aluminium salt of sucrose octa sulphate).2. Before you take GastalfetThere are no known contraindications.Take special care with GastalfetThe product should only be used with caution in patients with renal dysfunction.Taking other medicinesConcomitant use of sucralfate may reduce the bioavailability of certain drugs as has been observed in animal studies with tetracycline, phenytoin and cimetidine and in human studies with digoxin. Administration of Gastalfet with any of these drugs should be separated by two hours. Since sucralfate may hinder warfarin absorption, caution should be exercised when these two drugs are used together.Pregnancy and breast-feedingAlthough animal studies show no evidence of foetal malformation, safety in pregnant women has not been established and Gastalfet should be used in pregnancy only if clearly needed. It is not known whether this drug is excreted in human milk. Caution should be exercised when sucralfate is administered to nursing mothers.3. How to take Gastalfet?Taking this medicineAlways use Gastalfet exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.How much to take?Usual dose 1 gram 4 times daily to be taken 1 hour before meals and at bed time. Maximum daily dose is 8 grams.If you take more Gastalfet than you shouldIf you have too much of this medicine, talk to your doctor straight away.If you forget to take GastalfetIf you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten doseIf you stop taking GastalfetDo not stop taking this medicine without talking to your doctor. You should not stop taking Gastalfet just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsLike all medicines, Gastalfet can cause side effects, although not everybody gets them.The incidence and severity of side effects from sucralfate are very low. Mild side effect like constipation has been reported in some patients.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet5. How to store Gastalfet?Store in a cool and dry place, away from light.Keep out of reach of children..

Tk.4.02/=

  0 отзывов

Glipita 100 tablet

Glipita 100 tablet

What is Glipita?Glipita is the preparation of Sitagliptin. Sitagliptin is a new oral agent approved by the USFDA to treat type 2 diabetes with diet & exercise. It belongs to a new class of antihyperglycemic, Dipeptidyl Dipeptidase-4 (DPP-4) inhibitors. This unique class of orally active agent targets the underlying pathophysiologic processes of type 2 diabetic patients and provides an excellent alternative to the traditional agents.How Glipita works in our body?Normally, when glucose appears in blood after meal, Incretin hormones (GLP-1 & GIP) are secreted from gut to stimulate pancreatic β cell for insulin secretion and to act on α cell for glucagon inhibition. Dipeptidyl Peptidase 4 (DPP-4), an enzyme present in plasma, inactivates GLP-1 & GIP to stop insulin secretion from pancreatic β cell and to increase uninterrupted glucagon secretion from pancreatic α cell. Sitagliptin inhibits plasma DPP-4 activity (i.e. inactivation of GLP & GIP) and thus, increases circulating levels of active GLP-1 and GIP by two-to-threefold. This in turn, increases insulin release from pancreatic β cell and decreases glucagon levels from pancreatic α cell in the circulation in a glucose-dependent manner. Therefore, Sitagliptin is the only oral drug that involves both pancreatic α & β cell in a complimentary mode of action and thus ensures effective glycemic control in type 2 diabetes.What is the indications of Glipita?Monotherapy- GLIPITA is indicated as an adjunct to diet and exercise to improve glycemic control in patients with type 2 diabetes mellitus. Combination with Metformin- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with Metformin as initial therapy or when the single agent alone, with diet and exercise, does not provide adequate glycemic control. Combination with a Sulfonylurea- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with a sulfonylurea when treatment with the single agent alone, with diet and exercise, does not provide adequate glycemic control. Combination with a Thiazolidinediones- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with a thiazolidinedione when treatment with the single agent alone, with diet and exercise, does not provide adequate glycemic control. Combination with Metformin and a Sulfonylurea- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with Metformin and a sulfonylurea when dual therapy with these agents, with diet and exercise, does not provide adequate glycemic control.What is the dosage guideline for Glipita?The recommended dose of SITAGLIPTIN is 100 mg once daily as monotherapy or as combination therapy with Metformin, a sulfonylurea, a thiazolidinedione, or Metformin plus a sulfonylurea. SITAGLIPTIN can be taken with or without food. Patients with Renal Insufficiency- For patients with mild renal insufficiency (creatinine clearance [CrCl] ≥50 mL/min, approximately corresponding to serum creatinine levels of ≤1.7 mg/dL in men and ≤1.5 mg/dL in women), no dosage adjustment for SITAGLIPTIN is required. For patients with moderate renal insufficiency (CrCl ≥30 to <50 mL/min, approximately corresponding to serum creatinine levels of >1.7 to ≤3.0 mg/dL in men and >1.5 to ≤2.5 mg/dL in women), the dose of SITAGLIPTIN is 50 mg once daily. For patients with severe renal insufficiency (CrCl <30 mL/min, approximately corresponding to serum creatinine levels of >3.0 mg/dL in men and >2.5 mg/dL in women) or with end -stage renal disease (ESRD) requiring hemodialysis or peritoneal dialysis, the dose of SITAGLIPTIN is 25 mg once daily. SITAGLIPTIN may be administered without regard to the timing of hemodialysis. Concomitant Use with a Sulfonylurea- When SITAGLIPTIN is used in combination with a sulfonylurea, a lower dose of sulfonylurea may be required to reduce the risk of hypoglycemia. Patients with Hepatic Insufficiency- No dosage adjustment is necessary for patients with mild to moderate hepatic insufficiency. SITAGLIPTIN has not been studied in patients with severe hepatic insufficiency. Elderly- No dosage adjustment is necessary for elderly patients. Pediatric population- There is no data on the use of SITAGLIPTIN in patients younger than 18 years of age and therefore not recommended.Is there any dosage guideline for special population like renal insufficient patient with type 2 diabetes?Dosage adjustments in patients with moderate, severe, or end-stage renal disease (ESRD)50 mg once daily Moderate25 mg once daily Severe and ESRDCrCl ≥30 to <50 mL/min ˜Serum Cr levels (mg/dL)CrCl <30 mL/min ˜Serum Cr levels (mg/dL)Men: >1.7 – ≤3.0 Women: >1.5 – ≤2.5Men: >3.0 Women: >2.5 or on dialysisWhat are the precautions should I follow?SITAGLIPTIN should not be used in patients with type 1 diabetes or for the trea..

Tk.25.00/=

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Glipita 50 tablet

Glipita 50 tablet

Glipita 50 tabletWhat is Glipita?Glipita is the preparation of Sitagliptin. Sitagliptin is a new oral agent approved by the USFDA to treat type 2 diabetes with diet & exercise. It belongs to a new class of antihyperglycemic, Dipeptidyl Dipeptidase-4 (DPP-4) inhibitors. This unique class of orally active agent targets the underlying pathophysiologic processes of type 2 diabetic patients and provides an excellent alternative to the traditional agents.How Glipita works in our body?Normally, when glucose appears in blood after meal, Incretin hormones (GLP-1 & GIP) are secreted from gut to stimulate pancreatic β cell for insulin secretion and to act on α cell for glucagon inhibition. Dipeptidyl Peptidase 4 (DPP-4), an enzyme present in plasma, inactivates GLP-1 & GIP to stop insulin secretion from pancreatic β cell and to increase uninterrupted glucagon secretion from pancreatic α cell. Sitagliptin inhibits plasma DPP-4 activity (i.e. inactivation of GLP & GIP) and thus, increases circulating levels of active GLP-1 and GIP by two-to-threefold. This in turn, increases insulin release from pancreatic β cell and decreases glucagon levels from pancreatic α cell in the circulation in a glucose-dependent manner. Therefore, Sitagliptin is the only oral drug that involves both pancreatic α & β cell in a complimentary mode of action and thus ensures effective glycemic control in type 2 diabetes.What is the indications of Glipita?Monotherapy- GLIPITA is indicated as an adjunct to diet and exercise to improve glycemic control in patients with type 2 diabetes mellitus. Combination with Metformin- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with Metformin as initial therapy or when the single agent alone, with diet and exercise, does not provide adequate glycemic control. Combination with a Sulfonylurea- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with a sulfonylurea when treatment with the single agent alone, with diet and exercise, does not provide adequate glycemic control. Combination with a Thiazolidinediones- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with a thiazolidinedione when treatment with the single agent alone, with diet and exercise, does not provide adequate glycemic control. Combination with Metformin and a Sulfonylurea- GLIPITA is indicated in patients with type 2 diabetes mellitus to improve glycemic control in combination with Metformin and a sulfonylurea when dual therapy with these agents, with diet and exercise, does not provide adequate glycemic control.What is the dosage guideline for Glipita?The recommended dose of SITAGLIPTIN is 100 mg once daily as monotherapy or as combination therapy with Metformin, a sulfonylurea, a thiazolidinedione, or Metformin plus a sulfonylurea. SITAGLIPTIN can be taken with or without food. Patients with Renal Insufficiency- For patients with mild renal insufficiency (creatinine clearance [CrCl] ≥50 mL/min, approximately corresponding to serum creatinine levels of ≤1.7 mg/dL in men and ≤1.5 mg/dL in women), no dosage adjustment for SITAGLIPTIN is required. For patients with moderate renal insufficiency (CrCl ≥30 to <50 mL/min, approximately corresponding to serum creatinine levels of >1.7 to ≤3.0 mg/dL in men and >1.5 to ≤2.5 mg/dL in women), the dose of SITAGLIPTIN is 50 mg once daily. For patients with severe renal insufficiency (CrCl <30 mL/min, approximately corresponding to serum creatinine levels of >3.0 mg/dL in men and >2.5 mg/dL in women) or with end -stage renal disease (ESRD) requiring hemodialysis or peritoneal dialysis, the dose of SITAGLIPTIN is 25 mg once daily. SITAGLIPTIN may be administered without regard to the timing of hemodialysis. Concomitant Use with a Sulfonylurea- When SITAGLIPTIN is used in combination with a sulfonylurea, a lower dose of sulfonylurea may be required to reduce the risk of hypoglycemia. Patients with Hepatic Insufficiency- No dosage adjustment is necessary for patients with mild to moderate hepatic insufficiency. SITAGLIPTIN has not been studied in patients with severe hepatic insufficiency. Elderly- No dosage adjustment is necessary for elderly patients. Pediatric population- There is no data on the use of SITAGLIPTIN in patients younger than 18 years of age and therefore not recommended.Is there any dosage guideline for special population like renal insufficient patient with type 2 diabetes?Dosage adjustments in patients with moderate, severe, or end-stage renal disease (ESRD)50 mg once daily Moderate25 mg once daily Severe and ESRDCrCl ≥30 to <50 mL/min ˜Serum Cr levels (mg/dL)CrCl <30 mL/min ˜Serum Cr levels (mg/dL)Men: >1.7 – ≤3.0 Women: >1.5 – ≤2.5Men: >3.0 Women: >2.5 or on dialysisWhat are the precautions should I follow?SITAGLIPTIN should not be used in patients with type 1 diabete..

Tk.13.01/=

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Glipita M 50/1000 tablet

Glipita M 50/1000 tablet

Glipita M 50/1000 tabletWhat is Glipita-M?Glipita-M is the preparation of sitagliptin and metformin. Sitagliptin phosphate, a dipeptidyl peptidase 4(DPP-4) inhibitor and metformin HCI, a member of the biguanide class. Glipita-M is indicated as an adjunct to diet and exercise to treat Type 2 diabetes where metfromin is not enough to improve glycemic control. FDA Approves Glipita-M For Type 2 Diabetes, Offering Powerful Glucose Control Of A DPP-4 Inhibitor And Metformin in a Single Tablet.How Glipita works in our body?Glipita-M (sitagliptin phosphate/metformin HCI) combines 2 antihyperglycemic agents with complementary mechanism of action to improve glycemic control in patients with type 2 diabetes. Sitagliptin increases the levels of 2 known active incretin hormones, glucagon-like peptide-1(GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). When blood glucose concentrations are normal or elevated, GLP-1 and GIP increase insulin synthesis and release from pancreatic β-cells. GLP-1 also lowers glucagon secretion from pancreatic α-cells, leading to reduced hepatic glucose production. Metformin improves glucose tolerance in patients with type 2 diabetes, lowering both basal and postprandial plasma glucose. It decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization.What is the indications of Glipita-M?As initial therapy in type 2 DM when diet & exercise do not provide adequate glycemic control. As adjunct to diet & exercise to improve glycemic control in type 2 DM inadequately controlled on metformin or sitagliptin alone, or combination sitagliptin & metformin, or triple combination sitagliptin, metformin or a sulfonylurea.What are Dosage of Glipita-M?The dosage of Glipita-M should be individualized on the basis of the patient’s current regimen, effectiveness and tolerabilty while not excceding the maximum recommended daily dose of 100 mg sitagliptin and 2000 mg metformin. Initial combination therapy or maintenance of combination therapy should be individualized and left to the discretion of the health care provider . Glipita-M shoul generally be given twice daily with meals , with gradual dose escalation , to reducethe gasterointestinal side effect due to metformin. The recommended starting dose not currently treated with metformin is 50 mg sitagliptin/500 mg metformin hydrochloride twice daily, with gradual dose escalation recommended to reduce gastrointestinal side effects associated with metformin .The starting dose in patient already treated with metformin should provide sitagliptin dosed as 50 mg twice daily (100 mg toatal daily dose )and the dose of metformin already being taken. For patients taking 850 mg twice daily the recommended starting dose of Glipita-M is 50 mg sitagliptin/1000 mg metformin hydrochloride twice daily.Patients treated with an insulin secrtagauge or insulin co-administration of Glipita-M with an insulin secrtagauge (e.g. sulfonylurea) or insulin may require lower dose of insulin secretagauge or insulin to reduce the risk of hypoglycemia .No studies have been performed specifically examining the safety and efficacy of Glipita-M in patients previously treated with other oral antihyperglycemic agents and switched to Glipita-M.What is the Use of Glipita-M in Specific Populations:Pregnancy: Pregnancy Category B. There are no adequate and well-controlled studies in pregnant women with Sitagliptin/Metformin HCl combination or its individual components; therefore, the safety of Sitagliptin/Metformin HCl combination in pregnant women is not known. Nursing Mothers: No studies in lactating animals have been conducted with the combined components of Sitagliptin/Metformin HCl combination. Pediatric Use: Safety and effectiveness of Sitagliptin/Metformin HCl combination in pediatric patients under 18 years have not been established.Geriatric Use: Because sitagliptin and metformin are substantially excreted by the kidney, and because aging can be associated with reduced renal function, Sitagliptin/Metformin HCl combination should be used with caution as age increases. Care should be taken in dose selection and should be based on careful and regular monitoring of renal function.Selected Important Risk Information:Lactic acidosis is a rare but serious complication that can occur because of metformin accumulation. Glipita M is contraindicated in renal disease or renal dysfunction (serum creatinine levels >1.5 mg/dL in males and >1.4 mg/dL in females) or abnormal creatinine clearance.What are the possible adverse reactions of Glipita-M?Diarrhea, nausea, dyspepsia, flatulence, vomiting, headache, hypoglycaemia; abdominal pain, loss of appetite, metallic taste, hypersensitivity reactions...

Tk.16.00/=

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Glipita M 50/500 tablet

Glipita M 50/500 tablet

What is Glipita-M?Glipita-M is the preparation of sitagliptin and metformin. Sitagliptin phosphate, a dipeptidyl peptidase 4(DPP-4) inhibitor and metformin HCI, a member of the biguanide class. Glipita-M is indicated as an adjunct to diet and exercise to treat Type 2 diabetes where metfromin is not enough to improve glycemic control. FDA Approves Glipita-M For Type 2 Diabetes, Offering Powerful Glucose Control Of A DPP-4 Inhibitor And Metformin in a Single Tablet.How Glipita works in our body?Glipita-M (sitagliptin phosphate/metformin HCI) combines 2 antihyperglycemic agents with complementary mechanism of action to improve glycemic control in patients with type 2 diabetes. Sitagliptin increases the levels of 2 known active incretin hormones, glucagon-like peptide-1(GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). When blood glucose concentrations are normal or elevated, GLP-1 and GIP increase insulin synthesis and release from pancreatic β-cells. GLP-1 also lowers glucagon secretion from pancreatic α-cells, leading to reduced hepatic glucose production. Metformin improves glucose tolerance in patients with type 2 diabetes, lowering both basal and postprandial plasma glucose. It decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization.What is the indications of Glipita-M?As initial therapy in type 2 DM when diet & exercise do not provide adequate glycemic control. As adjunct to diet & exercise to improve glycemic control in type 2 DM inadequately controlled on metformin or sitagliptin alone, or combination sitagliptin & metformin, or triple combination sitagliptin, metformin or a sulfonylurea.What are Dosage of Glipita-M?The dosage of Glipita-M should be individualized on the basis of the patient’s current regimen, effectiveness and tolerabilty while not excceding the maximum recommended daily dose of 100 mg sitagliptin and 2000 mg metformin. Initial combination therapy or maintenance of combination therapy should be individualized and left to the discretion of the health care provider . Glipita-M shoul generally be given twice daily with meals , with gradual dose escalation , to reducethe gasterointestinal side effect due to metformin. The recommended starting dose not currently treated with metformin is 50 mg sitagliptin/500 mg metformin hydrochloride twice daily, with gradual dose escalation recommended to reduce gastrointestinal side effects associated with metformin .The starting dose in patient already treated with metformin should provide sitagliptin dosed as 50 mg twice daily (100 mg toatal daily dose )and the dose of metformin already being taken. For patients taking 850 mg twice daily the recommended starting dose of Glipita-M is 50 mg sitagliptin/1000 mg metformin hydrochloride twice daily.Patients treated with an insulin secrtagauge or insulin co-administration of Glipita-M with an insulin secrtagauge (e.g. sulfonylurea) or insulin may require lower dose of insulin secretagauge or insulin to reduce the risk of hypoglycemia .No studies have been performed specifically examining the safety and efficacy of Glipita-M in patients previously treated with other oral antihyperglycemic agents and switched to Glipita-M.What is the Use of Glipita-M in Specific Populations:Pregnancy: Pregnancy Category B. There are no adequate and well-controlled studies in pregnant women with Sitagliptin/Metformin HCl combination or its individual components; therefore, the safety of Sitagliptin/Metformin HCl combination in pregnant women is not known. Nursing Mothers: No studies in lactating animals have been conducted with the combined components of Sitagliptin/Metformin HCl combination. Pediatric Use: Safety and effectiveness of Sitagliptin/Metformin HCl combination in pediatric patients under 18 years have not been established.Geriatric Use: Because sitagliptin and metformin are substantially excreted by the kidney, and because aging can be associated with reduced renal function, Sitagliptin/Metformin HCl combination should be used with caution as age increases. Care should be taken in dose selection and should be based on careful and regular monitoring of renal function.Selected Important Risk Information:Lactic acidosis is a rare but serious complication that can occur because of metformin accumulation. Glipita M is contraindicated in renal disease or renal dysfunction (serum creatinine levels >1.5 mg/dL in males and >1.4 mg/dL in females) or abnormal creatinine clearance.What are the possible adverse reactions of Glipita-M?Diarrhea, nausea, dyspepsia, flatulence, vomiting, headache, hypoglycaemia; abdominal pain, loss of appetite, metallic taste, hypersensitivity reactions...

Tk.14.00/=

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Glucovis Eye Drops

Glucovis Eye Drops

Betaxolol Hydrochloride Ophthalmic Solution has the action of reducing elevated as well as normal intraocular pressure, whether or not accompanied by glaucoma.This preparation is used in lowering intraocular pressure and in the treatment of ocular hypertension and chronic open-angle glaucoma. The recommended dose is one to two drops of Betaxolol Hydrochloride Ophthalmic Solution in the affected eye(s) twice daily.Glucovis® eye drops should be used cautiously in diabetes mellitus, thyrotoxicosis, muscle weakness, major surgery, pulmonary, risk from anaphylactic reaction, carcinogenesis, mutagenesis, impairment of fertility.Betaxolol Hydrochloride Ophthalmic Solution should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Glucovis® 0.25% Eye Drops: Plastic dropper bottle containing 5 ml sterile solution. Each ml contains: Betaxolol Hydrochloride BP equivalent to Betaxolol 2.5 mg. ... reduces IOP and improves ocular blood flow with neuroprotective action Reduces elevated intraocular pressure.Improves ocular blood flow and provides neuroprotective action.Superior in visual field preservation in glaucoma patients.No evidence of cardiovascular beta –blocking action. Glucovis Eye Drops Prescribing InformationLocated in: Eye Care..

Tk.200.00/=

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Hemofix FZ 48/0.5/22.5 mg tablet

Hemofix FZ 48/0.5/22.5 mg tablet

Hemofix FZ tablet1. What Hemofix FZ is and what it is used for?It is an oral iron, folic acid and zinc preparation indicated for the treatment of iron, folic acid, and zinc deficiency.2. Before you take Hemofix FZDo not take this medicine and tell your doctor if:It is contraindicated in patients with haemolytic anaemia and in conditions with increased hypersensitivity to any of its components and increased body iron content.Take special care with Hemofix FZCare should be taken in patients who may develop iron overload, such as those with haemochromatosis, haemolytic anemia or red cell aplasia. Failure to respond to treatment may indicate other causes of anemia and should be further investigated.Taking other medicinesIron chelates with tetracycline, so this two product should not be taken within two hours of each other. Occasional gastrointestinal discomfort may be minimized by taking with meals. Absorption of iron may be impaired by concurrent administrations of penicillamine and antacid. In patients with renal failure, a risk of zinc accumulation may exist.Pregnancy and breast-feedingIf pregnant, or planning to become pregnant or are currently breast-feeding please contact your physician, before taking or continuing the drug. Administration in first trimester of pregnancy should be avoided unless definite evidence of iron deficiency is observed.3. How to take Hemofix FZ?Always use Hemofix FZ exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.How much to take?Adult & Elderly: One tablet a day before or after meal (food independent absorption) or as directed by the physician. In more severe cases, two tablets a day may be required as prescribed by the physician.If you take more Hemofix FZ than you shouldIf you have too much of this medicine, talk to your doctor straight away.If you forget to take Hemofix FZIf you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten doseIf you stop taking Hemofix FZDo not stop taking this medicine without talking to your doctor. You should not stop taking Hemofix FZ just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsSide effects of iron, folic acid and zinc supplementation are mild and transient. These include epigastric pain, nausea, constipation, vomiting, diarrhoea, heart burn, etc. Allergic sensitization has been reported following both oral and parenteral administration of folic acid.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet.5. How to store Hemofix FZ?Keep in a cool & dry place, protected from light. Keep out of the reach of children...

Tk.5.00/=

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Indelix SR Tab

Indelix SR Tab

1. What is and what it is used for? Indapamide is an oral antihypertensive agent. The pharmacological effects of indapamide in the treatment of hypertension include a reduction in cardiac hypertrophy and a reduction in the thickening of arterial walls. Indelix® SR is indicated in the treatment of essential hypertension. It is effective in treating hypertension in patients with renal function impairment, although its diuretic effect is reduced. Indelix® SR is also indicated for the treatment of salt and fluid retention associated with congestive heart failure.2. Before you take Indelix® SR? Do not take this medicine and tell your doctor if: This drug must not be taken in the conditions: Known allergy to this drug or to sulphonamides, Renal failure, Severe liver disease, Hypokalemia (abnormal decline in plasma potassium levels). Do not take this medicine if the above applies to you. If you are not sure, talk to your doctor before taking Indelix® SR. Take special care with Indelix® SR The drug should be used cautiously in disturbed water/ electrolyte balance, diabetes, gout and kidney problems. Monitoring of potassium and uric acid serum levels is also recommended. Taking other medicines Other Antihypertensive: No adverse reactions occur in combination with other antihypertensive drugs. Norepinephrine: Indapamide do not affect the effectiveness of norepinephrine. Pregnancy and breast-feeding There is no adequate and well-controlled studies in pregnant women and so indapamide is not recommended. Mothers taking indapamide should not breast feed. 3. How to take Indelix® SR? 1 tablet daily, preferably in the morning. In more severe cases, Indelix® SR can be combined with other categories of antihypertensive agents. If you take more Indelix® SR than you should In humans, experience with intentional overdosage of Indapamide is limited. If massive overdosage occurs, active cardiac and respiratory monitoring should be instituted. If you forget to take Indelix® SR If you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten dose If you stop taking Indelix® SR Do not stop taking this medicine without talking to your doctor. You should not stop taking Indelix SR just because you feel better. This is because the problem may come back or get worse again. If you have any further questions on the use of this product, ask your doctor or pharmacist. 4. Possible side effects Like all medicines, Indelix SR can cause side effects, although not everybody gets them. Side effects include dizziness, headache, anorexia, nausea, vomiting, constipation, diarrhea and postural hypotension. Electrolyte imbalances include hypochloremic alkalosis, hyponatremia, hypokalemia and hyperuricemia; hypersensitivity reactions which include skin rashes, cholestatic jaundice and blood dyscrasias including thrombocytopenia, leucopenia, aplastic anemia. Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet 5. How to store Indelix® SR? Keep in a cool and dry place. Protect from light. Located in: Cardiovascular..

Tk.6.00/=

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Inflavis Eye & Ear Drops

Inflavis Eye & Ear Drops

1. What Inflavis is and what it is used for (Mainly description as short form)? Inflavis eye drop contains Dexamethasone Phosphate 2. Before you take Inflavis? Do not take this medicine and tell your doctor if: Herpes simplex and other viral diseases of the cornea and conjunctiva, fungal disease, ocular tuberculosis, untreated purulent infections and hypersensitivity to any component of the preparation. Patients with soft contact lenses should not use this preparation.Take special care with Inflavis Check with your doctor before taking this medicine if: Topical corticosteroids should never be given for an undiagnosed red eye as inappropriate use is potentially blinding. Because of the risk of “steroid glaucoma” and cataract formation the intraocular pressure and the lens must be checked frequently during use of this preparation. To avoid the risk of enhancement of herpetic corneal disease, frequent slit-lamp examination is essential. Topical steroids may mask or enhance the activity of acute purulent eye infections. In such cases antibiotic therapy is mandatory. Persistent corneal ulceration following long-term topical steroid use may be due to fungal invasion. Taking other medicines None relevant to topical use. Pregnancy and breast-feeding There is inadequate evidence of safety in human pregnancy. Topical administration of corticosteroids to pregnant animals can cause abnormalities of foetal development including cleft palate and intra-uterine growth retardation. There may therefore be a very small risk of such effects in the human pregnancy. 3. How to take Inflavis(Administration)? Taking this medicine (Do not need to change) Always use Inflavis exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. How much to take? Eye: The frequency of instillation of drops and the duration of treatment will vary depending upon the severity of the underlying condition and the response to treatment. Severe inflammations require one to two drops instilled into the eye every thirty to sixty minutes until a satisfactory response occurs. If you take more Inflavis than you should If you have too much of this medicine, talk to your doctor straight away. If you forget to take Inflavis If you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten dose If you stop taking Inflavis Do not stop taking this medicine without talking to your doctor. You should not stop taking Inflavis just because you feel better. This is because the problem may come back or get worse again. If you have any further questions on the use of this product, ask your doctor or pharmacist. 4. Possible side effects Like all medicines, Inflavis can cause side effects, although not everybody gets them. Topical steroid use may result in increased intraocular pressure leading to optic nerve damage, reduced visual acuity and visual field defects. Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet 5. How to store? Store in a cool and dry place, away from light. Keep out of reach of children Inflavis Eye & Ear Drops Prescribing InformationLocated in: Eye Care..

Tk.70.00/=

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Informet XR 500mg Tab

Informet XR 500mg Tab

Informet LA 500 Tab..

Tk.6.00/=

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Intracef 15ml paediatric drops

Intracef 15ml paediatric drops

Intracef 15ml paediatric drops1. What Intracef is and what it is used for (Mainly description as short form)?Intracef contains Cefradine which is a semisynthetic first generation cephalosporin antibiotic that works in a similar way to penicillin by inhibiting bacterial cell wall synthesis.2. Before you take Intracef?Do not take this medicine and tell your doctor if:Patients with known hypersensitivity to cephalosporin antibiotics.3. Take special care with IntracefCheck with your doctor before taking this medicine if:There is evidence of partial cross allergenicity between penicillins and the cephalosporins. Therefore Cefradine should be used with caution in patients with known hypersensitivity to penicillins.4. Taking other medicinesThe cephalosporins are potentially nephrotoxic (particularly Cephaloridine) and may enhance the nephrotoxicity of aminoglycoside antibiotics such as Gentamicin and Tobramycin. One should be cautious about the use of any cephalosporin with urosemide and Ethacrynic acid.5. Pregnancy and breast-feedingPregnancy and lactation: No teratogenicity has been demonstrated in animals, but safety in pregnancy has not been established. Cefradine is excreted in breast milk and should be used with caution in lactating mothers.6. How to take IntracefIntracef may be given regardless of meals.Adults: For urinary tract infections the usual dose is 500 mg four times daily or 1 g twice daily; severe or chronic infections may require larger dose. Prolonged intensive therapy is needed for complications such as prostatitis and epididymitis. For respiratory tract infections and skin and soft tissue infections the usual dose is 250 mg or 500 mg four times daily or 500 mg or 1g twice daily depending on the severity and site of infection.Children: The usual dose is from 25 to 50 mg/kg/day total, given in two or four equally divided doses. For otitis media daily dose from 75 to 100 mg/kg body weight in divided doses every 6 to 12 hours are recommended. Maximum dose is 4 g per day.Elderly: There are no specific dosage recommendations or precautions for use in the elderly except as with other drugs to monitor those patients with impaired renal or hepatic function.Dosage in renal impairment:A modified dosage schedule is necessary in patients with decreased renal function. Each patient should be considered individually; the following modified dosage schedule is recommended as a guideline, based on the creatinine clearance (ml/min/1.73m2). In adults, the initial loading dose is 750 mg of Intracef and the maintenance dose is 500 mg at the time intervals listed below:Creatinine Clearance Time IntervalMore than 20 ml/min 6-12 hours15-19 ml/min 12-24 hours10-14 ml/min 24-40 hours5-9 ml/min 40-50 hoursLess than 5 ml/min 50-70 hoursFurther modification of the dosage schedule may be necessary in children.7. Possible side effectsRarely Cefradine may induce hypersensitivity reaction, nausea, vomiting, diarrhoea, glossitis, heartburn, dizziness, abdominal pain, candidal overgrowth, vaginitis, urticaria, skin rashes, joint pain and oedema. As with other cephalosporins, mild transient eosinophilia, leucopenia and neutropenia, rarely positive direct Coombs’ test and pseudomembraneous colitis have been reported.8. How to store Intracef?Store in a cool and dry place, away from light. Keep out of reach of children...

Tk.50.00/=

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Intracef 250 capsule

Intracef 250 capsule

1. What Intracef is and what it is used for (Mainly description as short form)?Intracef contains Cefradine which is a semisynthetic first generation cephalosporin antibiotic that works in a similar way to penicillin by inhibiting bacterial cell wall synthesis.2. Before you take Intracef?Do not take this medicine and tell your doctor if:Patients with known hypersensitivity to cephalosporin antibiotics.3. Take special care with IntracefCheck with your doctor before taking this medicine if:There is evidence of partial cross allergenicity between penicillins and the cephalosporins. Therefore Cefradine should be used with caution in patients with known hypersensitivity to penicillins.4. Taking other medicinesThe cephalosporins are potentially nephrotoxic (particularly Cephaloridine) and may enhance the nephrotoxicity of aminoglycoside antibiotics such as Gentamicin and Tobramycin. One should be cautious about the use of any cephalosporin with urosemide and Ethacrynic acid.5. Pregnancy and breast-feedingPregnancy and lactation: No teratogenicity has been demonstrated in animals, but safety in pregnancy has not been established. Cefradine is excreted in breast milk and should be used with caution in lactating mothers.6. How to take IntracefIntracef may be given regardless of meals.Adults: For urinary tract infections the usual dose is 500 mg four times daily or 1 g twice daily; severe or chronic infections may require larger dose. Prolonged intensive therapy is needed for complications such as prostatitis and epididymitis. For respiratory tract infections and skin and soft tissue infections the usual dose is 250 mg or 500 mg four times daily or 500 mg or 1g twice daily depending on the severity and site of infection.Children: The usual dose is from 25 to 50 mg/kg/day total, given in two or four equally divided doses. For otitis media daily dose from 75 to 100 mg/kg body weight in divided doses every 6 to 12 hours are recommended. Maximum dose is 4 g per day.Elderly: There are no specific dosage recommendations or precautions for use in the elderly except as with other drugs to monitor those patients with impaired renal or hepatic function.Dosage in renal impairment:A modified dosage schedule is necessary in patients with decreased renal function. Each patient should be considered individually; the following modified dosage schedule is recommended as a guideline, based on the creatinine clearance (ml/min/1.73m2). In adults, the initial loading dose is 750 mg of Intracef and the maintenance dose is 500 mg at the time intervals listed below:Creatinine Clearance Time IntervalMore than 20 ml/min 6-12 hours15-19 ml/min 12-24 hours10-14 ml/min 24-40 hours5-9 ml/min 40-50 hoursLess than 5 ml/min 50-70 hoursFurther modification of the dosage schedule may be necessary in children.7. Possible side effectsRarely Cefradine may induce hypersensitivity reaction, nausea, vomiting, diarrhoea, glossitis, heartburn, dizziness, abdominal pain, candidal overgrowth, vaginitis, urticaria, skin rashes, joint pain and oedema. As with other cephalosporins, mild transient eosinophilia, leucopenia and neutropenia, rarely positive direct Coombs’ test and pseudomembraneous colitis have been reported.8. How to store Intracef?Store in a cool and dry place, away from light. Keep out of reach of children...

Tk.6.50/=

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Intracef 500 capsule

Intracef 500 capsule

Intracef 500 capsule1. What Intracef is and what it is used for (Mainly description as short form)?Intracef contains Cefradine which is a semisynthetic first generation cephalosporin antibiotic that works in a similar way to penicillin by inhibiting bacterial cell wall synthesis.2. Before you take Intracef?Do not take this medicine and tell your doctor if:Patients with known hypersensitivity to cephalosporin antibiotics.3. Take special care with IntracefCheck with your doctor before taking this medicine if:There is evidence of partial cross allergenicity between penicillins and the cephalosporins. Therefore Cefradine should be used with caution in patients with known hypersensitivity to penicillins.4. Taking other medicinesThe cephalosporins are potentially nephrotoxic (particularly Cephaloridine) and may enhance the nephrotoxicity of aminoglycoside antibiotics such as Gentamicin and Tobramycin. One should be cautious about the use of any cephalosporin with urosemide and Ethacrynic acid.5. Pregnancy and breast-feedingPregnancy and lactation: No teratogenicity has been demonstrated in animals, but safety in pregnancy has not been established. Cefradine is excreted in breast milk and should be used with caution in lactating mothers.6. How to take IntracefIntracef may be given regardless of meals.Adults: For urinary tract infections the usual dose is 500 mg four times daily or 1 g twice daily; severe or chronic infections may require larger dose. Prolonged intensive therapy is needed for complications such as prostatitis and epididymitis. For respiratory tract infections and skin and soft tissue infections the usual dose is 250 mg or 500 mg four times daily or 500 mg or 1g twice daily depending on the severity and site of infection.Children: The usual dose is from 25 to 50 mg/kg/day total, given in two or four equally divided doses. For otitis media daily dose from 75 to 100 mg/kg body weight in divided doses every 6 to 12 hours are recommended. Maximum dose is 4 g per day.Elderly: There are no specific dosage recommendations or precautions for use in the elderly except as with other drugs to monitor those patients with impaired renal or hepatic function.Dosage in renal impairment:A modified dosage schedule is necessary in patients with decreased renal function. Each patient should be considered individually; the following modified dosage schedule is recommended as a guideline, based on the creatinine clearance (ml/min/1.73m2). In adults, the initial loading dose is 750 mg of Intracef and the maintenance dose is 500 mg at the time intervals listed below:Creatinine Clearance Time IntervalMore than 20 ml/min 6-12 hours15-19 ml/min 12-24 hours10-14 ml/min 24-40 hours5-9 ml/min 40-50 hoursLess than 5 ml/min 50-70 hoursFurther modification of the dosage schedule may be necessary in children.7. Possible side effectsRarely Cefradine may induce hypersensitivity reaction, nausea, vomiting, diarrhoea, glossitis, heartburn, dizziness, abdominal pain, candidal overgrowth, vaginitis, urticaria, skin rashes, joint pain and oedema. As with other cephalosporins, mild transient eosinophilia, leucopenia and neutropenia, rarely positive direct Coombs’ test and pseudomembraneous colitis have been reported.8. How to store Intracef?Store in a cool and dry place, away from light. Keep out of reach of children...

Tk.12.50/=

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Intracef DS susp.

Intracef DS susp.

Intracef DS susp.1. What Intracef is and what it is used for (Mainly description as short form)?Intracef contains Cefradine which is a semisynthetic first generation cephalosporin antibiotic that works in a similar way to penicillin by inhibiting bacterial cell wall synthesis.2. Before you take Intracef?Do not take this medicine and tell your doctor if:Patients with known hypersensitivity to cephalosporin antibiotics.3. Take special care with IntracefCheck with your doctor before taking this medicine if:There is evidence of partial cross allergenicity between penicillins and the cephalosporins. Therefore Cefradine should be used with caution in patients with known hypersensitivity to penicillins.4. Taking other medicinesThe cephalosporins are potentially nephrotoxic (particularly Cephaloridine) and may enhance the nephrotoxicity of aminoglycoside antibiotics such as Gentamicin and Tobramycin. One should be cautious about the use of any cephalosporin with urosemide and Ethacrynic acid.5. Pregnancy and breast-feedingPregnancy and lactation: No teratogenicity has been demonstrated in animals, but safety in pregnancy has not been established. Cefradine is excreted in breast milk and should be used with caution in lactating mothers.6. How to take IntracefIntracef may be given regardless of meals.Adults: For urinary tract infections the usual dose is 500 mg four times daily or 1 g twice daily; severe or chronic infections may require larger dose. Prolonged intensive therapy is needed for complications such as prostatitis and epididymitis. For respiratory tract infections and skin and soft tissue infections the usual dose is 250 mg or 500 mg four times daily or 500 mg or 1g twice daily depending on the severity and site of infection.Children: The usual dose is from 25 to 50 mg/kg/day total, given in two or four equally divided doses. For otitis media daily dose from 75 to 100 mg/kg body weight in divided doses every 6 to 12 hours are recommended. Maximum dose is 4 g per day.Elderly: There are no specific dosage recommendations or precautions for use in the elderly except as with other drugs to monitor those patients with impaired renal or hepatic function.Dosage in renal impairment:A modified dosage schedule is necessary in patients with decreased renal function. Each patient should be considered individually; the following modified dosage schedule is recommended as a guideline, based on the creatinine clearance (ml/min/1.73m2). In adults, the initial loading dose is 750 mg of Intracef and the maintenance dose is 500 mg at the time intervals listed below:Creatinine Clearance Time IntervalMore than 20 ml/min 6-12 hours15-19 ml/min 12-24 hours10-14 ml/min 24-40 hours5-9 ml/min 40-50 hoursLess than 5 ml/min 50-70 hoursFurther modification of the dosage schedule may be necessary in children.7. Possible side effectsRarely Cefradine may induce hypersensitivity reaction, nausea, vomiting, diarrhoea, glossitis, heartburn, dizziness, abdominal pain, candidal overgrowth, vaginitis, urticaria, skin rashes, joint pain and oedema. As with other cephalosporins, mild transient eosinophilia, leucopenia and neutropenia, rarely positive direct Coombs’ test and pseudomembraneous colitis have been reported.8. How to store Intracef?Store in a cool and dry place, away from light. Keep out of reach of children...

Tk.120.00/=

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Intracef susp.

Intracef susp.

Intracef susp.1. What Intracef is and what it is used for (Mainly description as short form)?Intracef contains Cefradine which is a semisynthetic first generation cephalosporin antibiotic that works in a similar way to penicillin by inhibiting bacterial cell wall synthesis.2. Before you take Intracef?Do not take this medicine and tell your doctor if:Patients with known hypersensitivity to cephalosporin antibiotics.3. Take special care with IntracefCheck with your doctor before taking this medicine if:There is evidence of partial cross allergenicity between penicillins and the cephalosporins. Therefore Cefradine should be used with caution in patients with known hypersensitivity to penicillins.4. Taking other medicinesThe cephalosporins are potentially nephrotoxic (particularly Cephaloridine) and may enhance the nephrotoxicity of aminoglycoside antibiotics such as Gentamicin and Tobramycin. One should be cautious about the use of any cephalosporin with urosemide and Ethacrynic acid.5. Pregnancy and breast-feedingPregnancy and lactation: No teratogenicity has been demonstrated in animals, but safety in pregnancy has not been established. Cefradine is excreted in breast milk and should be used with caution in lactating mothers.6. How to take IntracefIntracef may be given regardless of meals.Adults: For urinary tract infections the usual dose is 500 mg four times daily or 1 g twice daily; severe or chronic infections may require larger dose. Prolonged intensive therapy is needed for complications such as prostatitis and epididymitis. For respiratory tract infections and skin and soft tissue infections the usual dose is 250 mg or 500 mg four times daily or 500 mg or 1g twice daily depending on the severity and site of infection.Children: The usual dose is from 25 to 50 mg/kg/day total, given in two or four equally divided doses. For otitis media daily dose from 75 to 100 mg/kg body weight in divided doses every 6 to 12 hours are recommended. Maximum dose is 4 g per day.Elderly: There are no specific dosage recommendations or precautions for use in the elderly except as with other drugs to monitor those patients with impaired renal or hepatic function.Dosage in renal impairment:A modified dosage schedule is necessary in patients with decreased renal function. Each patient should be considered individually; the following modified dosage schedule is recommended as a guideline, based on the creatinine clearance (ml/min/1.73m2). In adults, the initial loading dose is 750 mg of Intracef and the maintenance dose is 500 mg at the time intervals listed below:Creatinine Clearance Time IntervalMore than 20 ml/min 6-12 hours15-19 ml/min 12-24 hours10-14 ml/min 24-40 hours5-9 ml/min 40-50 hoursLess than 5 ml/min 50-70 hoursFurther modification of the dosage schedule may be necessary in children.7. Possible side effectsRarely Cefradine may induce hypersensitivity reaction, nausea, vomiting, diarrhoea, glossitis, heartburn, dizziness, abdominal pain, candidal overgrowth, vaginitis, urticaria, skin rashes, joint pain and oedema. As with other cephalosporins, mild transient eosinophilia, leucopenia and neutropenia, rarely positive direct Coombs’ test and pseudomembraneous colitis have been reported.8. How to store Intracef?Store in a cool and dry place, away from light. Keep out of reach of children...

Tk.80.00/=

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Ipramid HFA Inhaler

Ipramid HFA Inhaler

Ipramid is a preperation of Ipratropium bromide which is a anticholinergic agent that works as a bronchodilator that dilates the bronchi in the lungs. It is used in treating chronic obstructive pulmonary disease associated with chronic bronchitis and emphysema. In chronic obstructive pulmonary disease, cholinergic nerves going to the lungs cause narrowing of the bronchi by stimulating the muscles surrounding the bronchi to contract. An “anti-cholinergic” effect of ipratropium bromide blocks the effect of the cholinergic nerves, causing the muscles to relax and the bronchi to dilate.Ensures excellent bronchodilation in COPDOffers a specific therapy of COPDShows additive effect with salbutamol and theophyllineRight choice for elderly COPD patientsOffers an alternative bronchodilator option in asthma   ( Respirator Solution Ipratropium Bromide 250 mcg/ml ) Ipratropium bromide is an anticholinergic bronchodilator. It inhibits vagally mediated reflexes by antagonizing, the action of acetylcholine, the transmitter agent released from the vagal nerve. Ipratropium Prescribing InformationLocated in: Respiratory ..

Tk.220.00/=

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Iprasol HFA Inhaler

Iprasol HFA Inhaler

Iprasol is a preperation of Salbutamol & Ipratropium bromide.Salbutamol is a beta2-adrenergic agent which acts on airway smooth muscle resulting in relaxation. Ipratropium Bromide is a anticholinergic agent that works as a bronchodilator that dilates the bronchi in the lungs. Iprasol provides the simultaneous release of ipratropium bromide and salbutamol allowing the synergistic efficacy on the muscarinic and beta2-adrenergic receptors in the airways to cause bronchodilation which is superior to that provided by each single agent and with no potentiation of adverse events.Dual mechanism of action offers more bronchodilation than Salbutamol and Ipratropium alone in specific situationsReduces hypersecretion and increase bronchial muscle tone through anticholinergic pathwayAn effective and safe alternative to Nebulizer as emergency treatment both at home and emergency department (with large volume spacer)Two therapy in one inhaler increases patients’ compliance Iprasol HFA Prescribing InformationLocated in: Respiratory..

Tk.250.00/=

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Iprasol Respirator Solution 20 ml

Iprasol Respirator Solution 20 ml

Iprasol is a preparation of Salbutamol & Ipratropium bromide.Salbutamol is a beta2-adrenergic agent which acts on airway smooth muscle resulting in relaxation. Ipratropium Bromide is a anticholinergic agent that works as a bronchodilator that dilates the bronchi in the lungs. Iprasol provides the simultaneous release of ipratropium bromide and salbutamol allowing the synergistic efficacy on the muscarinic and beta2-adrenergic receptors in the airways to cause bronchodilation which is superior to that provided by each single agent and with no potentiation of adverse events.Offers definite relief to the patients in asthma & COPDEnsures treatment adherence & patients? complianceAn effective & safer alternative to nebulizer both in home & emergency setting Iprasol Prescribing Information   ( Ipratropium Bromide 0.5 mg and Salbutamol 2.5 mg/ml Respirator Solution ) This Inhalation Solution is a combination of the anticholinergic bronchodilator, ipratropium bromide, and the ß2-adrenergic bronchodilator, salbutamol sulfate. Ipratropium bromide is a quaternary ammonium derivative of atropine and is an anticholinergic drug which has bronchodilator properties. On inhalation, the onset of action is noted within 5 to 15 minutes, with a peak response between 1 and 2 hours, lasting about 2 additional hours, with subsequent decline from the peak. Bronchodilation is still evident 8 hours after inhalation. Salbutamol produces bronchodilation through stimulation of ß2-adrenergic receptors in bronchial smooth muscle, thereby causing relaxation of muscle fibres. This action is manifested by an increase in pulmonary function as demonstrated by spirometric measurements. A measurable decrease in airway resistance is typically observed 5 to 15 minutes after inhalation of salbutamol. The maximum improvement in pulmonary function usually occurs after 60 to 90 minutes, and significant bronchodilator activity has been observed to persist from 3 to 6 hours. Ipratropium Bromide Prescribing InformationLocated in: Respiratory..

Tk.225.00/=

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Jointec Max tablet

Jointec Max tablet

Jointec Max tabletWhat Jointec® Max is and what it is used for?Jointec® Max is a combination of Diacerein and Glucosamine for the treatment of osteoarthritis and joint pain. Diacerein is a new anti inflammatory drug developed specially for the treatment of Osteoarthritis. It directly inhibits IL-1 beta synthesis and release in vitro and down modulates IL-1 induced activities and have been shown to possess disease modifying effect in experimental models of osteoarthritis and in human subjects with finger joint and knee osteoarthritis. Glucosamine sulfate is a naturally occurring chemical found in the human body.Before you take Jointec® MaxIt is contraindicated in patients suffering from diarrhea or having sensitivity regarding any of its components.How to take Jointec® Max?Always use Jointec® Max exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.How much to take?Adult and Children 12 years and older: The usual dose of Jointec® Max is 1 tablet twice daily (12 hourly) It should be taken with food.If you forget to take Jointec® MaxIf you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten dose.If you stop taking Jointec® MaxDo not stop taking this medicine without talking to your doctor. You should not stop taking Jointec® Max just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.Possible side effectsDiarrhea, constipation, epigastria pain, heartburn, nausea, vomiting, headache, skin rashes, drowsiness.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet.How to store Jointec® Max (Storage condition)Keep in a cool & dry place, protected from light. Keep out of the reach of children. Jointec Max Prescribing Information..

Tk.12.00/=

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Keolax Tablet

Keolax Tablet

Clobazam® is a benzodiazepine derivative with action and uses similar to those of Diazepam. Absorption of clobazam is virtually complete after oral administration. Keolax® is indicated for the relief of acute or chronic anxiety, tension and agitation. The recommended oral dose is 20-30 mg daily in divided doses or as a single dose given at night.Ensures a trouble free anxiolytic therapyTreats seizures effectivelyEnsures quick relief from anxietyEnsures safety from treatment Keolax Prescribing InformationLocated in: Central Nervous System..

Tk.2.77/=

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Koloride 1000 ml

Koloride 1000 ml

1. What Koloride is and what it is used for? Koloride is a sterile solution of Sodium Chloride, Potassium Chloride and Sodium Acetate. Koloride contains different electrolytes which are usually depleted in various conditions e.g. diarrhoea, vomiting, profuse sweating etc. So, Koloride is indicated in cholera, also in diarrhoea, vomiting, fluid loss, to replenish and restore the normal electrolyte balance of the body. 2. Before you take Koloride Take special care with Koloride Check with your doctor before taking this medicine if: Since Cholera Saline contains different electrolytes, it should be infused with caution in patients where electrolyte imbalance may cause detrimental effects, e.g. in pregnancy, renal impairment, heart failure, pulmonary congestion, head injury etc. or in patients receiving potassium sparing diuretics.3. How to take Koloride? Taking this medicine. Always use Koloride exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. How much to take? The volume and rate of infusion of Cholera Saline depends upon the requirements of the patient and the judgement of the physician. It usually varies with age, weight and clinical condition of the patient. 4. Possible side effects Severe burning, pain, or swelling around the IV needle;Warmth, redness, oozing, or bleeding where the IV was placed;fever, ongoing cough; Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet 5. How to store Koloride? Koloride should be stored at controlled room temperature. Koloride Prescribing InformationLocated in: Intravenous Fluids..

Tk.91.72/=

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Koloride 500ml IV infution

Koloride 500ml IV infution

1. What Koloride is and what it is used for? Koloride is a sterile solution of Sodium Chloride, Potassium Chloride and Sodium Acetate. Koloride contains different electrolytes which are usually depleted in various conditions e.g. diarrhoea, vomiting, profuse sweating etc. So, Koloride is indicated in cholera, also in diarrhoea, vomiting, fluid loss, to replenish and restore the normal electrolyte balance of the body. 2. Before you take Koloride Take special care with Koloride Check with your doctor before taking this medicine if: Since Cholera Saline contains different electrolytes, it should be infused with caution in patients where electrolyte imbalance may cause detrimental effects, e.g. in pregnancy, renal impairment, heart failure, pulmonary congestion, head injury etc. or in patients receiving potassium sparing diuretics.3. How to take Koloride? Taking this medicine. Always use Koloride exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. How much to take? The volume and rate of infusion of Cholera Saline depends upon the requirements of the patient and the judgement of the physician. It usually varies with age, weight and clinical condition of the patient. 4. Possible side effects Severe burning, pain, or swelling around the IV needle;Warmth, redness, oozing, or bleeding where the IV was placed;fever, ongoing cough; Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet 5. How to store Koloride? Koloride should be stored at controlled room temperature. Koloride Prescribing InformationLocated in: Intravenous Fluids..

Tk.70.14/=

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Lacrison-T Eye Drops

Lacrison-T Eye Drops

Lacrison®-T is the preparation of Loteprednol etabonate which is belongs to a group of medicines known as steroidal anti-inflammatory drugs and Tobramycin which is a broad spectrum antibiotic. Lacrison®-T is indicated for steroid-responsive inflammatory ocular conditions for which a corticosteroid is indicated and where superficial bacterial ocular infection or a risk of bacterial ocular infection exists.Before you take Lacrison®-T?Do not take this medicine and tell your doctor if: you are allergic to any ingredient in Lacrison®-T drops or to similar medicines, including corticosteroids or aminoglycoside antibiotics.you have a viral disease in the eye, including herpes simplex keratitis (dendritic keratitis), vaccinia, or varicellayou have a mycobacterial or fungal infection of the eyeyou are breast-feeding Contact your doctor or health care provider right away if any of these apply to you. Take special care with Lacrison®-TCheck with your doctor before taking this medicine if you suffer from, or have in the past suffered from: Tell your doctor if you already have glaucomaTell your doctor if pain develops, or if redness, itching, or inflammation gets worseSee your doctor if your symptoms do not get better within 2 days. He/she may want to re-evaluate your conditionProlonged use of corticosteroids may result in glaucoma with damage to the optic nerve, and defects in visual acuity and fields of vision. Steroids should be used with caution in the presence of glaucoma. If this product is used for 10 days or longer, intraocular pressure should be monitored.Use of corticosteroids may result in posterior subcapsular cataract formationLong-term use of this medicine or other eye drops that contain steroids, may lower your ability to fight infections and may increase your chance of getting an eye infection including herpes simplexUsing steroid eye drops like medicine may make viral diseases of the eye worse and last longer Taking other medicinesSome MEDICINES MAY INTERACT with Lacrison®-T Eye drops. Tell your health care provider if you are taking any other medicines, especially any of the following:Certain diuretic medicines (eg, furosemide), cyclosporine, nonsteroidal anti-inflammatory medicines (NSAIDs) (eg, ibuprofen), or other medicines containing aminoglycoside antibiotics (eg, tobramycin, gentamicin) because the risk of their side effects may be increased by this eye drops. Pregnancy and breast-feedingIf you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine as steroids may be harmful to the baby. 3. How to take Lacrison®-T (Administration)?Always use this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure. How much to take?Apply 1 or 2 drops of Lacrison®-T into the conjunctival sac of the affected eye every 4 to 6 hours. During the initial 24 to 48 hours, the dosing may be increased, to every 1 to 2 hours. Frequency should be decreased gradually as warranted by improvement in clinical signs. Care should be taken not to discontinue therapy prematurely. If you take more Lacrison®-T than you shouldPutting too many drops in your eye(s) is unlikely to lead to unwanted side effects. Tell your doctor or a pharmacist. If you forget to take Lacrison®-T If you forget to take a dose, take it as soon as you remember it. However, if it is nearly time for the next dose, skip the missed dose. Do not take a double dose to make up for a forgotten dose If you stop taking Lacrison®-T Always use this medicine exactly as your doctor has told you. Do not stop using Lacrison®-T without speaking to your doctor first. If you have any further questions on the use of this medicine, ask your doctor or pharmacist. 4. Possible side effectsAll medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:Burning or stinging upon using Lacrison®-T Eye drops; mild itching, discomfort, or redness of the eye.Seek medical attention right away if any of these SEVERE side effects occur:Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision or other vision changes; sensitivity to light; severe or worsening pain or inflammation, redness, swelling, or discharge from the eye or eyelid; unusual tearing. This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. 5. How to store?Keep this medicine out of the sight and reach of children.Discard the bottle 28 days after opening, even if there is solution remaining.Do not store above 25°C (room temperature). Do not freeze. Lacrison-®T Eye Drops Prescribing InformationLocated in: Eye Care..

Tk.200.00/=

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Lactameal susp.

Lactameal susp.

Lactameal susp.Lactameal® is an antacid containing a combination of Aluminium hydroxide B.P as gel) and Magnesium Hydroixde B.P. It is indicated in hyperacidity, gastric ulcer duodenal ulcer and gastritis.A perfectly controlled acid neutralizerProvides safety to patientsKeeps the product stable until shelf lifeConfirms therapeutic actionEnsures the patients' compliance to therapy Lactameal Prescribing Information..

Tk.33.10/=

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Lactameal tablet

Lactameal tablet

Lactameal tabletLactameal® is an antacid containing a combination of Aluminium hydroxide B.P as gel) and Magnesium Hydroixde B.P. It is indicated in hyperacidity, gastric ulcer duodenal ulcer and gastritis.A perfectly controlled acid neutralizerProvides safety to patientsKeeps the product stable until shelf lifeConfirms therapeutic actionEnsures the patients' compliance to therapy Lactameal Prescribing Information..

Tk.0.73/=

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Lactoride 1000 ml infuson

Lactoride 1000 ml infuson

Lactoride 1000 ml infuson1. What Lactoride is and what it is used for?Lactoride is a sterile solution of Sodium Chloride, Potassium Chloride, Calcium Chloride and Sodium Lactate. Lactoride is used to treat hypovolemia caused by surgery, hemorrhage and trauma. Excessive sweating, severe diarrhoea or vomiting, excess loss of fluid by nephrotic kidneys, inadequate intake of fluid and electrolytes etc. that may lead to typical hypovolemic shock may be corrected with Lactoride. Severe plasma loss caused by intestinal obstruction, burns or other denuding conditions of the skin may be treated with Lactoride. Lactoride is mainly used as a fluid and electrolyte replenisher. It may be used as an alternative to Sodium Bicarbonate in the treatment of metabolic acidosis associated with dehydration and to alkalinize urine.2. Before you take LactorideDo not take this medicine and tell your doctor if:Hartmann's solution may be relatively contraindicated in patients with diabetes mellitus, as one of the isomers of lactate is gluconeogenic.Take special care with LactorideCheck with your doctor before taking this medicine if:Lactoride should not be administered rapidly or for prolonged periods. Since the solution contains different electrolytes, it should be infused with caution in patients where electrolyte imbalance may cause detrimental effects; e.g. in pregnancy, renal impairment, heart failure, pulmonary congestion, etc. or to patients receiving potassium sparing diuretics.Pregnancy and breast-feedingPregnancy Category C. Animal reproduction studies have not been conducted with Lactated Ringer’s Irrigation. It is also not known whether it can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. It should be given to a pregnant woman only if clearly needed.3. How to take Lactoride?Taking this medicine. Always use Lactoride exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.How much to take?The volume and rate of infusion will depend upon the requirements of the patients and the judgement of the physician. It usually varies with age, weight and clinical condition of the patient. The recommended flow rate is up to 100-drops/minute/70 kg body weight. In burn patients the dose of Lactoride according to the Parkland formula : 4ml/kg body weight/% of Body surface area (BSA) burn (e.g. for a 30% BSAburn of a person having 60 kg body weight, 4 x 60x30ml = 7200 ml of Lactoride would be required in 24 hours). Half of this within 8 hr, the remainder over 16 hr.4. Possible side effectsHands, ankles and feet may become mildly swollen from fluid retention. Rarely, the lungs can also be affected, which may cause breathing difficulty. Other possible symptoms include nausea, vomiting, headache, dizziness, drowsiness, confusion, and inflammation or swelling of the veins around the site of the injection.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet5. How to store Lactoride?Lactoride should be stored at controlled room temperature. Lactoride Prescribing Information..

Tk.91.72/=

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lactoride 500 ml

lactoride 500 ml

lactoride 500 ml1. What Lactoride is and what it is used for?Lactoride is a sterile solution of Sodium Chloride, Potassium Chloride, Calcium Chloride and Sodium Lactate. Lactoride is used to treat hypovolemia caused by surgery, hemorrhage and trauma. Excessive sweating, severe diarrhoea or vomiting, excess loss of fluid by nephrotic kidneys, inadequate intake of fluid and electrolytes etc. that may lead to typical hypovolemic shock may be corrected with Lactoride. Severe plasma loss caused by intestinal obstruction, burns or other denuding conditions of the skin may be treated with Lactoride. Lactoride is mainly used as a fluid and electrolyte replenisher. It may be used as an alternative to Sodium Bicarbonate in the treatment of metabolic acidosis associated with dehydration and to alkalinize urine.2. Before you take LactorideDo not take this medicine and tell your doctor if:Hartmann's solution may be relatively contraindicated in patients with diabetes mellitus, as one of the isomers of lactate is gluconeogenic.Take special care with LactorideCheck with your doctor before taking this medicine if:Lactoride should not be administered rapidly or for prolonged periods. Since the solution contains different electrolytes, it should be infused with caution in patients where electrolyte imbalance may cause detrimental effects; e.g. in pregnancy, renal impairment, heart failure, pulmonary congestion, etc. or to patients receiving potassium sparing diuretics.Pregnancy and breast-feedingPregnancy Category C. Animal reproduction studies have not been conducted with Lactated Ringer’s Irrigation. It is also not known whether it can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. It should be given to a pregnant woman only if clearly needed.3. How to take Lactoride?Taking this medicine. Always use Lactoride exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.How much to take?The volume and rate of infusion will depend upon the requirements of the patients and the judgement of the physician. It usually varies with age, weight and clinical condition of the patient. The recommended flow rate is up to 100-drops/minute/70 kg body weight. In burn patients the dose of Lactoride according to the Parkland formula : 4ml/kg body weight/% of Body surface area (BSA) burn (e.g. for a 30% BSAburn of a person having 60 kg body weight, 4 x 60x30ml = 7200 ml of Lactoride would be required in 24 hours). Half of this within 8 hr, the remainder over 16 hr.4. Possible side effectsHands, ankles and feet may become mildly swollen from fluid retention. Rarely, the lungs can also be affected, which may cause breathing difficulty. Other possible symptoms include nausea, vomiting, headache, dizziness, drowsiness, confusion, and inflammation or swelling of the veins around the site of the injection.Tell your doctor if any of the side effects gets serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet5. How to store Lactoride?Lactoride should be stored at controlled room temperature. Lactoride Prescribing Information..

Tk.71.09/=

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Limogel ointment

Limogel ointment

Limogel® is a preparation of Lysine hydrochloride. It is an essential amino acid & soluble in water. It promotes healing of wounds by active and controlled regeneration of cells. It also protects the wounds against common organisms. It plays an important role in the formation of collagen, a substance important for bones and connective tissues including skin, tendon, and cartilage. Lysine is important for proper growth, and it plays an essential role in the production of carnitine, a nutrient responsible for converting fatty acids into energy and helping to lower cholesterol. It is indicated in the prevention of infection in cuts, wounds abrasions, surgical incisions, burns, advance chronic wounds and infected traumatic lesions.Heals wound naturallyEffective against burn and accidental woundsProvides quick relief from cold sores Limogel Prescribing InformationLocated in: Skin Care..

Tk.80.00/=

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Liveric 150 tablet

Liveric 150 tablet

Liveric 150 tabletLiveric® is a preparation Ursodeoxycholic Acid, one of the secondary bile acids. It is used to dissolve gallstones made of cholesterol and is the only USFDA approved drug to treat primary biliary cirrhosis.Ursodeoxycholic acid is known to reduce cholesterol content of biliary fluid (produced by the liver and stored in the gall bladder for secretion into the intestine to digest fats) and also to reduce the absorption of cholesterol from the gut. Both of these actions decrease the amount of cholesterol that passes into the bile. Also, since Ursodeoxycholic Acid is a bile acid itself, it increases the level of bile acids within the bile. The combination of these two factors stops the cholesterol separating out of the bile. The gallstones then begin to dissolve. This is a useful alternative for people who cannot have, or wish to avoid surgery. Liveric Prescribing Information..

Tk.11.03/=

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Liveric 300

Liveric 300

Liveric 300Liveric® is a preparation Ursodeoxycholic Acid, one of the secondary bile acids. It is used to dissolve gallstones made of cholesterol and is the only USFDA approved drug to treat primary biliary cirrhosis.Ursodeoxycholic acid is known to reduce cholesterol content of biliary fluid (produced by the liver and stored in the gall bladder for secretion into the intestine to digest fats) and also to reduce the absorption of cholesterol from the gut. Both of these actions decrease the amount of cholesterol that passes into the bile. Also, since Ursodeoxycholic Acid is a bile acid itself, it increases the level of bile acids within the bile. The combination of these two factors stops the cholesterol separating out of the bile. The gallstones then begin to dissolve. This is a useful alternative for people who cannot have, or wish to avoid surgery. Liveric Prescribing Information..

Tk.20.06/=

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Lofat 200 mg capsule

Lofat 200 mg capsule

What Lofat® capsules are and what they are used for?Lofat® is a preparation of Fenofibrate that belongs to a group of medicines, commonly known as fibrates. These medicines are used to lower the level of fats (lipids) in the blood. For example, the fats known as triglycerides. Lofat® (Fenofibrate) capsules are used, alongside a low fat diet and other non-medical treatments such as exercise and weight loss, to lower levels of fats in the blood.Lofat®(Fenofibrate) capsules can be used in addition to other medicines (statins) in some circumstances when levels of fats in the blood are not controlled with a statin alone.What you need to know before you take Lofat® capsules Do not take Lofat® (Fenofibrate) capsules and tell your doctor if you: are allergic to fenofibrate or any of the other ingredients in the capsules.have developed a sensitivity to sunlight or artificial light (e.g. sunbeds) when taking fibrates (e.g. fenofibrate or bezafibrate) or ketoprofen (used for muscle and bone disorders, gout or period pain).have severely impaired liver function.have gallbladder or liver disease.have severe kidney problems.have problems with your pancreas.are giving Fenofibrate capsules to a child or adolescent. Lofat® (Fenofibrate) capsules must not be used in children and adolescents under 18. Warnings and precautions Talk to your doctor or pharmacist before taking Lofat® (Fenofibrate) capsules if you: have had impaired kidney function.have severely increased levels of a type of fat (triglycerides) in the blood (severe hypertriglyceridemia) (seen in a blood test).have any of the following which may increase the risk of you developing abnormal muscle breakdown: impaired kidney functionan underactive thyroida high alcohol intakeare over 70 years oldhave had or have a family member with a history of hereditary muscular disorders. have decreased levels of a certain protein in the blood (hypoalbuminemia) (seen in a blood test).are already taking a fibrate (e.g. bezafibrate) or a statin (e.g. atorvastatin), especially if you have muscle disease.have poorly controlled diabetes mellitus (type II).have nephrotic syndrome characterized by large amounts of protein in the urine, water retention and increased levels of fats in the blood.have a condition which effects the amount of protein in the blood (dysproteinemia).have obstructive liver disease.are taking medicines which may affect fat metabolism (e.g. thiazides, beta blockers, corticosteroids or antiretrovirals). Other medicines and Lofat® capsules Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines especially: oral anti-coagulants e.g. warfarin (used to prevent blood clotting).statins e.g. atorvastatin- used to lower cholesterol.cyclosporine- used to suppress the immune system.phenylbutazone- a non-steroidal anti-inflammatory drug.other fibrates e.g. bezafibrate- used to lower cholesterol and other fats (lipids) in the blood.estrogen or medicines which contain estrogen (contraceptives). Pregnancy and breast-feeding Fenofibrate capsules should not be used if you are pregnant or breast-feeding. If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. Lofat® capsules contain lactose If you have been told you have an intolerance to some sugars, contact your doctor before taking this medicine, as it contains a type of sugar called lactose. Tests Your doctor may want to carry out tests to monitor the levels of certain enzymes within your body. How to take Lofat® capsules? Taking this medicine Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. Swallow the capsules whole with water during a meal. How much to take? Adults: One capsule a day. Your doctor will monitor your response to the treatment. Elderly: No dose modifications necessary for this age group. Children and adolescents: Lofat® (Fenofibrate) capsules must not be used in children and adolescents under 18. Impaired kidney function If you have impaired kidney function, your doctor may prescribe you a lower dose. If you take more than you should If you (or someone else) swallow a lot of capsules at the same time, or you think a child may have swallowed any, contact your nearest hospital emergency department or tell your doctor immediately. If you forget to take the capsules Do not take a double dose to make up for a forgotten dose. If you forget to take a dose, take it as soon as you remember it and then take the next dose at the right time. Possible side effects Like all medicines, this medicine can cause side effects, although not everybody gets them. Stop taking Lofat® (Fenofibrate) capsules and tell your doctor immediately if you develop: Muscle poisoning: muscle pain, breakdown, inflammation, cramps or weakness, increa..

Tk.7.00/=

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Lospan 10 tablet

Lospan 10 tablet

Lospan 10 tablet1. What Lospan is and what it is used for?Lospan (Baclofen) is a centrally acting skeletal muscle relaxant and an antispastic agent with a spinal site of action.Lospan is indicated for the signs and symptoms of spasticity resulting from multiple sclerosis, particularly for the relief of flexor spasms and concomitant pain, clonus, and muscular rigidity, spinal cord injuries and other spinal cord diseases.2. Before you take LospanDo not take this medicine and tell your doctor if:Lospan is contraindicated in patients with hypersensitivity to any component of this product.Take special care with LospanCheck with your doctor before taking this medicine if:Patients should also be cautioned that the central nervous system effects of baclofen may be additive to those of alcohol and other CNS depressants. It is not known whether this drug is excreted in human milk. As a general rule, nursing should not be undertaken while a patient is on a drug since many drugs are excreted in human milk.Taking other medicinesAlcohol and other CNS depressants may exacerbate the CNS effects of baclofen and should be avoided, severe aggravation of hyperkinetic symptoms may possibly occur in patients taking lithium.Pregnancy and breast-feedingThere are no adequate and well controlled studies of Baclofen in pregnant women. So it should be used during pregnancy only if the potential benefit outweighs the potential risk to the fetus.Baclofen is excreted in breast milk. However, evidence suggests that the quantities are so small that no undesirable effect on the infant would be expected.3. How to take Lospan?The determination of optimal dosage requires individual titration. The following dosage titration schedule is suggested: 5 mg t.i.d. for 3 days, 10 mg t.i.d. for 3 days, 15 mg t.i.d. for 3 days, 20 mg t.i.d. for 3 days. Thereafter additional increases may be necessary but the total daily dose should not exceed a maximum of 80 mg daily.If you forget to take LospanIf you forget to take a dose, take it as soon as you remember it. If it is almost time for your next dose, do not take the missed dose. Take the next dose on time.If you stop taking LospanDo not stop taking this medicine without talking to your doctor. You should not stop taking Lospan just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.4. Possible side effectsLike all medicines, Lospan can cause side effects, although not everybody gets them.The most common side-effects include drowsiness, nausea, dizziness, lightheadedness, confusion, fatigue, muscular pain and weakness, and hypotension.5. How to store Lospan?Store in a cool and dry place, away from light.Keep out of reach of children. Lospan Prescribing Information..

Tk.8.00/=

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Loverin tablet

Loverin tablet

Dicycloverine Hydrochloride (Dicyclomine Hydrochloride) is a tertiary amine used to prevent gastrointestinal smooth muscle spasm. It works due to its antimuscarinic effects. Loverin is indicated for Symptomatic relief of gastrointestinal disorders characterized by smooth muscle spasm. Each tablet contains Dicycloverine Hydrochloride BP 10 mg.Single agent to treat multiple spastic conditions Works effectively against contraction & spasm thus reduces spasm related abdominal painEffective antispasmodic for infantile colicSafer antispasmodic in pregnancy(USFDA pregnancy category B) Loverin Prescribing InformationLocated in: Gastrointestinal..

Tk.2.01/=

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