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 Adora Powder for Suspension

Adora Powder for Suspension

IndicationsAdora (Cefadroxil Monohydrate) is indicated for the treatment of patients with infection caused by susceptible strains of the designated organisms in the following diseases: *Upper respiratory tract infections caused by Streptococcus pyogenes (Group A beta-hemolytic Streptococci) and Streptococcus pneumoniae. * Urinary tract infections caused by E. coli, Proteus mirabilis, and Klebsiella species. * Skin and soft tissue infections caused by Staphylococci (including penicillinase producing strains) and Streptococci.  DescriptionsAdora (Cefadroxil Monohydrate) is an acid-stable semi-synthetic oral antibiotic in the cephalosporin family of drugs. Cefadroxil acts by preventing bacteria from forming protective cell wall necessary for survival. It has superior pharmacokinetic profile over all first generation cephalosporins.Dosage & AdministrationThe bioavailability and consequent chemotherapeutic effects of Cefadroxil are unaffected by foods. It may, therefore, be taken with meals or on an empty stomach. Administration with food may be helpful in diminishing potential gastrointestinal complaints occasionally associated with oral cephalosporin therapy.Side EffectsGenerally cefadroxil is well tolerated. However, the most commonly reported side effects are gastrointestinal disturbances and hypersensitivity phenomena. Side effects including nausea, vomiting, diarrhoea, dyspepsia, abdominal discomfort, fever, dizziness, headache, arthralgia may also occur. PrecautionN/AContraindicationsCefadroxil is contraindicated in patients with a history of hypersensitivity to any of the ingredientUse in Pregnancy & LactationCefadroxil (Adora) is widely used as a first-line oral antibiotic for the treatment of uncomplicated urinary tract infections in pregnant women.Drug InteractionThere is no known clinically important drug interactions with Cefadroxil.OverdoseIf amounts >250 mg/kg is ingested, gastric lavage or simulation of vomiting is appropriate.Commercial PackagingAdora 500 mg Capsule : Box containing 5 Alu-Alu blister strips of 4 capsules. Adora Powder for Suspension : Bottle containing powder to produce 100 ml suspension when reconstituted. Adora Powder for Suspension : Bottle containing powder to produce 60 ml suspension when reconstituted. Adora Powder for Paediatric Drops: Bottle containing powder for preparation of 15 ml suspension.OthersDirection for Reconstitution of suspension For 100 ml suspension and 100 ml DS suspension: Add 65 ml (13 measuring spoonful) of boiled and cooled water to the dry mixture in the bottle. For ease of preparation add water to the bottle in two portions. Shake well after each addition until all the powder is in suspension. For 60 ml suspension: Add 40 ml (8 measuring spoonful) of boiled and cooled water to the dry mixture in the bottle. For ease of preparation add water to the bottle in two portions. Shake well after each addition until all the powder is in suspension. Paediatric Drops: Add 10 ml (2 measuring spoonful) to the bottle and shake vigorously. Note: Shake both oral suspension and paediatric drops well before each use. Keep the bottle tightly closed. The reconstituted suspension should be stored in a cool and dry place, preferably in refrigerator and unused portion should be discarded after 14 days...

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 Radirif 2 injection

Radirif 2 injection

Indication: Moderate to severe pain, moderate to severe pain associated with myocardial infarction (MI), as a supplement to balanced anesthesia, for preoperative and postoperative analgesia and for obstetrical analgesia during labor and delivery.Dosage & Administration:The usual recommended adult dose is 10 mg for a 70 kg individual, administered subcutaneously, intramuscularly or intravenously; this dose may be repeated every 3 to 6 hours as necessary. Dosage should be adjusted according to the severit..

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Acuren (Tab) 25mg/tablet

Acuren (Tab) 25mg/tablet

IndicationsHydrochlorothiazide is indicated in – • Edema associated with congestive heart failure, hepatic cirrohosis, various forms of renal dysfunction and corticosteroid and estrogen therapy • Management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe form of hypertension • Management of diabetes insipidus • Management of proximal renal tubular acidosis • Idiopathic hypercalciuria and calcium nephrolithiasis, osteoporosis and exercise induced hyperkalemiaDescriptionsHydrochlorothiazide is a novel diuretic which affects the distal renal tubular mechanism of electrolyte reabsorption. Hydrochlorothiazide increases excretion of sodium and chloride in approximately equivalent amounts. The mechanism of the antihypertensive effect of thiazides is unknown. Hydrochlorothiazide does not usually affect normal blood pressure.Dosage & AdministrationAdults For Edema: The usual adult dosage is 25 to 100 mg daily as a single or divided dose. For Control of Hypertension: The usual initial dose in adults is 25 mg daily given as a single dose. The dose may be increased to 50 mg daily, given as a single or two divided doses. Doses above 50 mg are often associated with marked reductions in serum potassium. In some patients (especially the elderly) an initial dose of 12.5 mg daily may be sufficient. Infants and children For diuresis and for control of hypertension: The usual pediatric dosage is 1 to 2 mg per kg body weight per day in single or two divided doses, not to exceed 37.5 mg per day in infants up to 2 years of age or 100 mg per day in children 2 to 12 years of age. In infants less than 6 months of age, doses up to 3 mg per kg body weight per day in two divided doses may be required.Side EffectsGenerally, Hydrochlorothiazide is well tolerated. However, a few side effects may occur like weakness, restlessness, dizziness, headache, fever, diarrhea, vomiting, sialadenitis, cramping, constipation, gastric irritation, nausea, anorexia, and hypotension. In rare case hyperglycemia, glycosuria, hyperuricemia and muscle spasm may occur.PrecautionsThiazides should be used with caution in patients with severe renal disease, impaired hepatic function or progressive liver disease and gout.ContraindicationsHydrochlorothiazide is contraindicated to the patients of anuria and those who are sensitive to hydrochlorothiazide or to other sulfonamide-derived drugs. Therapy is not to be initiated in diabetes mellitus.Use in Pregnancy & LactationPregnancy: Evidence of fetal risk in hydrochlorothiazide therapy is found, but it is indicated if benefits outweigh risks. Thiazides are indicated in pregnancy when edema is due to pathologic causes. Lactation: Neonatal side effects have been seen incase of hydrochlorothiazide therapy and therefore it is not recommended.Drug InteractionAlcohol, Barbiturates, or Narcotics: Potentiation of orthostatic hypotension may occur. Antidiabetic Drugs (oral agents and insulin): Thiazides can impair control of diabetes mellitus by diet and antidiabetic Drugs. Antihypertensive Drugs: Additive effect or potentiation.OverdoseThe most common signs and symptoms observed are those caused by electrolyte depletion (hypokalemia, hypochloremia, hyponatremia) and dehydration resulting from excessive diuresis. Rarely, autoimmune hemolytic anemia and other hypersensitivity reactions may complicate the picture. In the event of over dosage, symptomatic and supportive measures should be employed. Emesis should be induced or gastric lavage performed. Correct dehydration, electrolyte imbalance, hepatic coma and hypotension by established procedures. Hemodialysis can be used successfully to treat severe intoxication.Commercial PackagingAcuren 25: Each box contains 10 blister strips of 10 tablets. Acuren 50: Each box contains 10 blister strips of 10 tablets...

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Acuren (Tab) 50mg/tablet

Acuren (Tab) 50mg/tablet

IndicationsHydrochlorothiazide is indicated in – • Edema associated with congestive heart failure, hepatic cirrohosis, various forms of renal dysfunction and corticosteroid and estrogen therapy • Management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe form of hypertension • Management of diabetes insipidus • Management of proximal renal tubular acidosis • Idiopathic hypercalciuria and calcium nephrolithiasis, osteoporosis and exercise induced hyperkalemiaDescriptionsHydrochlorothiazide is a novel diuretic which affects the distal renal tubular mechanism of electrolyte reabsorption. Hydrochlorothiazide increases excretion of sodium and chloride in approximately equivalent amounts. The mechanism of the antihypertensive effect of thiazides is unknown. Hydrochlorothiazide does not usually affect normal blood pressure.Dosage & AdministrationAdults For Edema: The usual adult dosage is 25 to 100 mg daily as a single or divided dose. For Control of Hypertension: The usual initial dose in adults is 25 mg daily given as a single dose. The dose may be increased to 50 mg daily, given as a single or two divided doses. Doses above 50 mg are often associated with marked reductions in serum potassium. In some patients (especially the elderly) an initial dose of 12.5 mg daily may be sufficient. Infants and children For diuresis and for control of hypertension: The usual pediatric dosage is 1 to 2 mg per kg body weight per day in single or two divided doses, not to exceed 37.5 mg per day in infants up to 2 years of age or 100 mg per day in children 2 to 12 years of age. In infants less than 6 months of age, doses up to 3 mg per kg body weight per day in two divided doses may be required.Side EffectsGenerally, Hydrochlorothiazide is well tolerated. However, a few side effects may occur like weakness, restlessness, dizziness, headache, fever, diarrhea, vomiting, sialadenitis, cramping, constipation, gastric irritation, nausea, anorexia, and hypotension. In rare case hyperglycemia, glycosuria, hyperuricemia and muscle spasm may occur.PrecautionsThiazides should be used with caution in patients with severe renal disease, impaired hepatic function or progressive liver disease and gout.ContraindicationsHydrochlorothiazide is contraindicated to the patients of anuria and those who are sensitive to hydrochlorothiazide or to other sulfonamide-derived drugs. Therapy is not to be initiated in diabetes mellitus.Use in Pregnancy & LactationPregnancy: Evidence of fetal risk in hydrochlorothiazide therapy is found, but it is indicated if benefits outweigh risks. Thiazides are indicated in pregnancy when edema is due to pathologic causes. Lactation: Neonatal side effects have been seen incase of hydrochlorothiazide therapy and therefore it is not recommended.Drug InteractionAlcohol, Barbiturates, or Narcotics: Potentiation of orthostatic hypotension may occur. Antidiabetic Drugs (oral agents and insulin): Thiazides can impair control of diabetes mellitus by diet and antidiabetic Drugs. Antihypertensive Drugs: Additive effect or potentiation.OverdoseThe most common signs and symptoms observed are those caused by electrolyte depletion (hypokalemia, hypochloremia, hyponatremia) and dehydration resulting from excessive diuresis. Rarely, autoimmune hemolytic anemia and other hypersensitivity reactions may complicate the picture. In the event of over dosage, symptomatic and supportive measures should be employed. Emesis should be induced or gastric lavage performed. Correct dehydration, electrolyte imbalance, hepatic coma and hypotension by established procedures. Hemodialysis can be used successfully to treat severe intoxication.Commercial PackagingAcuren 25: Each box contains 10 blister strips of 10 tablets. Acuren 50: Each box contains 10 blister strips of 10 tablets...

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Adora Powder for Paediatric Drops

Adora Powder for Paediatric Drops

IndicationsAdora (Cefadroxil Monohydrate) is indicated for the treatment of patients with infection caused by susceptible strains of the designated organisms in the following diseases: *Upper respiratory tract infections caused by Streptococcus pyogenes (Group A beta-hemolytic Streptococci) and Streptococcus pneumoniae. * Urinary tract infections caused by E. coli, Proteus mirabilis, and Klebsiella species. * Skin and soft tissue infections caused by Staphylococci (including penicillinase producing strains) and Streptococci.  DescriptionsAdora (Cefadroxil Monohydrate) is an acid-stable semi-synthetic oral antibiotic in the cephalosporin family of drugs. Cefadroxil acts by preventing bacteria from forming protective cell wall necessary for survival. It has superior pharmacokinetic profile over all first generation cephalosporins.Dosage & AdministrationThe bioavailability and consequent chemotherapeutic effects of Cefadroxil are unaffected by foods. It may, therefore, be taken with meals or on an empty stomach. Administration with food may be helpful in diminishing potential gastrointestinal complaints occasionally associated with oral cephalosporin therapy.Side EffectsGenerally cefadroxil is well tolerated. However, the most commonly reported side effects are gastrointestinal disturbances and hypersensitivity phenomena. Side effects including nausea, vomiting, diarrhoea, dyspepsia, abdominal discomfort, fever, dizziness, headache, arthralgia may also occur. PrecautionN/AContraindicationsCefadroxil is contraindicated in patients with a history of hypersensitivity to any of the ingredientUse in Pregnancy & LactationCefadroxil (Adora) is widely used as a first-line oral antibiotic for the treatment of uncomplicated urinary tract infections in pregnant women.Drug InteractionThere is no known clinically important drug interactions with Cefadroxil.OverdoseIf amounts >250 mg/kg is ingested, gastric lavage or simulation of vomiting is appropriate.Commercial PackagingAdora 500 mg Capsule : Box containing 5 Alu-Alu blister strips of 4 capsules. Adora Powder for Suspension : Bottle containing powder to produce 100 ml suspension when reconstituted. Adora Powder for Suspension : Bottle containing powder to produce 60 ml suspension when reconstituted. Adora Powder for Paediatric Drops: Bottle containing powder for preparation of 15 ml suspension.OthersDirection for Reconstitution of suspension For 100 ml suspension and 100 ml DS suspension: Add 65 ml (13 measuring spoonful) of boiled and cooled water to the dry mixture in the bottle. For ease of preparation add water to the bottle in two portions. Shake well after each addition until all the powder is in suspension. For 60 ml suspension: Add 40 ml (8 measuring spoonful) of boiled and cooled water to the dry mixture in the bottle. For ease of preparation add water to the bottle in two portions. Shake well after each addition until all the powder is in suspension. Paediatric Drops: Add 10 ml (2 measuring spoonful) to the bottle and shake vigorously. Note: Shake both oral suspension and paediatric drops well before each use. Keep the bottle tightly closed. The reconstituted suspension should be stored in a cool and dry place, preferably in refrigerator and unused portion should be discarded after 14 days...

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Alervil Syrup

Alervil Syrup

DescriptionAlervil is suitable for the treatment of hypersensitivity reactions and pruritus of varying origin.IndicationsIn different allergic conditions (hypersensitivity reactions) such as:* Seasonal and perennial rhinitis;* Hay fever (pollinosis) with attacks of sneezing, itching, running of the nose;*Conjunctivitis;* Different skin allergies like; dermatitis, eczema, urticaria, angioedema;* Pruritus of various etiology;* Vasomotor rhinitis;* Vertigo.Dosage & AdministrationAlervil syrup is particularly suitable for children.Children aged 1-3 years should receive half a measuring spoonful 2 or 3 times daily.Children aged 4-12 years: 1 measuring spoonful 2 or 3 times daily.Adults and young people: 1-2 measuring spoonful of syrup 2 or 3 times a day after meals.A daily dose of 3mg/kg body weight must not be exceeded.Side EffectsOccasionally there may be drowsiness, gastrointestinal complaints, dryness of mouth, palpitation, urinary retention or hypersensitivity reactions. In isolated cases, higher doses may produce hallucinations, restlessness or confusion; in small children, agitation. In patients with narrow angle-glaucoma a rise in intraocular pressure is possible, which makes opthalmologic control necessary. Even if used according to prescription, these preparations may reduce alertness to such an extent that the ability to cope with street traffic or operate machinery is impaired.PrecautionsDuring pregnancy and lactation, pheniramine should be used only if strictly indicated,and after considering the benefit/risk ratio for mother and child.Drug InteractionThe effect of drugs which act on the central nervous system (e.g. tranquilizers, sedatives, neuroleptic agents and MAO inhibitors) and of alcohol may be potentiated...

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Alurol 100mg tablet

Alurol 100mg tablet

Indications• In the management of primary gout or secondary hyperuricaemia associated with chronic gout. In severe cases of chronic gout, Allopurinol can be used together with a uricosuric agent unless the latter is contra-indicated. • Uric acid nephropathy • Recurrent uric acid stone formation • Certain enzyme disorders or blood disorders which lead to overproduction of urate (e.g., Lesch-Nyhan syndrome, hemolytic anaemia) • Hyperuricaemia associated with malignancy and cytotoxic therapy which results in a high cell turnover rate • The prevention and treatment of calcium oxalate/phosphate renal stones in the presence of high uric acid levels of the blood and/or urine.DescriptionsAlurol is used to decrease uric acid concentrations in plasma and/or urine when hyperuricaemia is clinically significant. Alurol and its active metabolite oxypurinol inhibit xanthine oxidase, the enzyme responsible for the conversion of hypoxanthine to xanthine to uric acid. Inhibition of this enzyme accounts for the major pharmacological effects of Alurol. In contrast with the uricosuric agents that increase the renal excretion of urate, Alurol inhibits the terminal steps in uric acid biosynthesis. 90% of the Alurol from tablets is absorbed in the gastro-intestinal tract. The Alurol is rapidly metabolized to the active metabolite oxypurinol (alloxanthine). After administration, peak plasma levels occur generally at 1.5 hrs for Alurol. It has a plasma half-life of approximately 1 hour.Dosage & AdministrationAllopurinol may be taken once daily after a meal. It is normally well tolerated especially after food. Should the total daily dose exceed 300 mg and/or gastro-intestinal intolerance be manifested, a divided doses regimen may be appropriate. The dosage should be adjusted by monitoring serum urate concentrations and urinary urate/uric acid levels at appropriate intervals. Adults The average daily dose is 2-10 mg/kg body weight or 100 mg to 200 mg for mild conditions, 300 mg to 600 mg daily for moderate severe conditions and 700 to 900 mg for severe conditions. Initial therapy: Allopurinol may increase the frequency of acute attacks during the first few months of therapy; it is therefore recommended that low doses be given initially and slowly increased, and that anti-inflammatory agents or colchicines should be given concomitantly during this period as prophylactic cover. In patients with renal function, doses of 100 mg should be given and increased by 50 mg to 100 mg at weekly intervals until serum levels of 0.6 mg per ml are achieved. Hyperuricaemia of malignancy or cancer therapy: Therapy should be initiated 2 to 3 days prior to cytotoxic therapy after which maintenance doses are given according to response. Adequate hydration is essential throughout. Children Hyperuricaemia associated with malignancy: 6-10 years: 300 mg daily Under 6 years: 150 mg daily Impaired renal function: 100-200 mg dailySide EffectsThe most common side effect is skin rash. Fever, chills, leucopenia, eosinophilia, arthalgia, nausea, vomiting, abdominal pain, diarrhea, alopecia, headache, drowsiness and peripheral neuritis are other side effects.PrecautionsAllopurinol should be discontinued at the first sign of a rash or other sign of immediate allergic reactions. It is not recommended for the treatment of mild asymptomatic hyperuricaemia.It should generally only be considered if serum urate concentrations exceed 0.8 to 0.9 mg/ml with an aim of reducing levels to 0.6 mg/ml.ContraindicationsAcute gout and allergy to Allopurinol.Use in Pregnancy & LactationCategory B2. Although animal studies have not indicated any incidence of teratogenicity, the effect of Allopurinol on the human fetus is unknown and it should be used in pregnancy only if clearly needed. Allopurinol is distributed into breast milk. It should be used with caution in view of the potential for hypersensitivity reactions.Drug InteractionAllopurinol may increase the incidence of skin rash in patients taking Ampicillin. Aluminium hydroxide, as the antacid can reduce the absorption of Allopurinol.OverdoseNausea, vomiting, diarrhea and dizziness have been reported who ingested 20 gm Allopurinol. The patient should be monitored and receive normal supportive measures and should be adequately hydrated to maintain urinary excretion of allopurinol and its metabolites.Commercial PackagingAlurol 100 mg tablet: Each box contains 10 blister strips of 10 tablets..

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ANGIFIX 20 Tab.

ANGIFIX 20 Tab.

Indications Isosorbide mononitrate tablets are indicated for- The prevention of angina pectoris due to coronary artery disease. The onset of action of oral isosorbide mononitrate is not sufficiently rapid for this product to be useful in aborting an acute anginal episode.Long-term treatment of blood-flow disorders of the coronary vessels (coronary heart disease)Long-term treatment and prophylaxis of angina pectoris (chest pain due to coronary blood-flow disorders of the coronary vessels).Treatment of severe myocardial insufficiency (chronic heart failure) Therapeutic Class Nitrates: Coronary vasodilators Description Isosorbide-5-mononitrate is an active metabolite of isosorbide dinitrate. It is a vasodilator with effects on both arteries and vein and also coronary vessels. It causes reduction of preload and afterload and redistributes coronary flow to ischemic regions. Pharmacology Isosorbide mononitrate relaxes vascular smooth muscles by stimulating cyclic-GMP. It decreases left ventricular pressure (preload) and arterial resistance (afterload). Dosage & Administration The recommended regimen of Isosorbide Mononitrate tablets is 20 mg (one tablet) twice daily, with the two doses given 7 hours apart. For most patients, this can be accomplished by taking the first dose on awakening and the second dose 7 hours later. Dosage adjustments are not necessary for elderly patients or patients with altered renal or hepatic function. Multiple studies of organic nitrates have shown that maintenance of continuous 24-hour plasma levels results in refractory tolerance. The dosing regimen for Isosorbide Mononitrate tablets provides a daily nitrate-free interval to avoid the development of this tolerance. Well-controlled studies have shown that tolerance to Isosorbide Mononitrate tablets is avoided when using the twice-daily regimen in which the two doses are given 7 hours apart. This regimen has been shown to have antianginal efficacy beginning 1 hour after the first dose and lasting at least 5 hours after the second dose. The duration (if any) of antianginal activity beyond 12 hours has not been studied; large controlled studies with other nitrates suggest that no dosing regimen should be expected to provide more than about 12 hours of continuous antianginal efficacy per day.In clinical trials, Isosorbide Mononitrate tablets have been administered in a variety of regimens. Single doses less than 20 mg have not been adequately studied, while single doses greater than 20 mg have demonstrated no greater efficacy than doses of 20 mg. Interaction Hypotensive effects may be increased when used with alcohol or vasodilators. Concurrent use with calcium channel blockers may lead to marked orthostatic hypotension. Contraindications It is contraindicated in patients who have shown hypersensitivity or idiosyncratic reactions to other nitrates or nitrites. Side Effects Hypotension, tachycardia, flushing, headache, dizziness, palpitation, syncope, confusion. Nausea, vomiting, abdominal pain. Restlessness, weakness and vertigo. Dry mouth, chest pain, back pain, oedema, fatigue, abdominal pain, constipation, diarrhoea, dyspepsia and flatulence. Pregnancy & Lactation There are no adequate and controlled studies to date with Isosorbide-5-mononitrate in pregnant women, and the drug should be used during pregnancy only when the potential benefit justified possible risks to the fetus. Execration of Isosorbide-5-mononitrate into human milk is unknown, so precaution should be taken when it is administered to a nursing mother. Precautions Severe renal or severe hepatic impairment, hypothyroidism, malnutrition, or hypothermia. Caution in patients who are already hypotensive. May aggravate angina caused by hypertrophic cardiomyopathy. Tolerance may develop after long-term treatment. Lactation. ..

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Ansulin R (100 IU/ml) Pen Cartridge

Ansulin R (100 IU/ml) Pen Cartridge

Indication: Type 1 and Type 2 Diabetes Mellitus.Dosage & Administration:The dosage form, the dosage and the administration time of the insulin are different due to the individual differences of each patient. In addition, the dosage is also affected by food, working style and exercising intensity. Therefore, patients should use the insulin under doctor\'s instruction. The average range of total daily insulin requirement for maintenance therapy in type 1 diabetic patients lies between 0.5 and 1.0 IU/kg. In pre-pubertal children it usually varies from 0.7 to 1.0 IU/kg, whereas in insulin resistant cases, e.g. during puberty or due to obesity, the daily insulin requirement may be substantially higher. Initial dosages for type 2 diabetic patients are often lower, e.g. 0.3 to 0.6 IU/kg/day...

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Aquaphen Syrup

Aquaphen Syrup

Indications This is indicated for the symptomatic relief of upper respiratory tract disorders accompanied by productive cough which benefits from the administration of a nasal decongestant, a histamine H1 receptor antagonist and an expectorant combination. Therapeutic Class Combined cough expectorants Pharmacology Pseudoephedrine is a decongestant as well as a bronchodilator for the upper respiratory tract, which gives symptomatic relief of nasal congestion. Pseudoephedrine is both an α-and β-adrenergic receptor agonist. It causes vasoconstriction via direct stimulation of α-adrenergic receptors of the respiratory mucosa. It also directly stimulates β-adrenergic receptors causing bronchial relaxation, increased heart rate and contractility.Like ephedrine, pseudoephedrine releasing norepinephrine from its storage sites, an indirect effect. This is its main and direct mechanism of action. The displaced noradrenaline is released into the neuronal synapse where it is free to activate the postsynaptic adrenergic receptors.Guaifenesin reduces the viscosity of tenacious sputum and is used as an expectorant. It increases the hydration of respiratory tract, thereby increasing the volume and reducing the viscosity of bronchial secretions.Triprolidine is an antihistamine; it is used for the symptomatic relief of hypersensitivity reactions including rhinitis, conjunctivitis and urticaria. Dosage & Administration Adult and Children over 12 years: 10 ml (2 teaspoonful) three times a day.Children 6-12 years: 5 ml (1 teaspoonful) three times a day.Children 2-5 years: 2.5 ml (1/2 teaspoonful) three times a day.A physician’s advice is preferred before administering this preparation to children aged less than 2 years. Interaction Concomitant use of Pseudoephedrine, guaiphenasine & triprolidine with sympathomimetic agents such as decongestants, tricyclic antidepressants, appetite suppressants and amphetamine-like psychostimulants or with monoamine oxidase inhibitors which interfere with the catabolism of sympathomimetic amines may occasionally cause a rise in blood pressure. Because of its pseudoephedrine content, Pseudoephedrine, guaiphenasine & triprolidine partially reverse the hypotensive action of drugs which interfere with sympathetic activity including guanethidine, methyldopa, alpha-adrenergic blocking agents. Contraindications This is contraindicated in the cases of known hypersensitivity to any of its constituents, cardiovascular disease including hypertension, lower respiratory symptoms including asthma, monoamine oxidase inhibitor (MAOI) therapy. Side Effects CNS depression or excitation, drowsiness (reported most frequently), sleep disturbances, hallucinations (rarely reported), skin rashes with or without irritation, tachycardia, dryness of mouth, nose and throat have occasionally been reported. Pregnancy & Lactation Although pseudoephedrine, triprolidine and guaiphenesin have been in widespread use of many years without apparent ill consequence, there are no specific data on their use during pregnancy. Caution should therefore be exercised by balancing the potential benefits of treatment of the mother against any possible hazards to the developing fetus. Precautions As with any other antihistamine therapy, Pseudoephedrine, guaiphenasine & triprolidine may cause drowsiness. If affected, patients should be advised not to drive or operate machinery. Concomitant administration of alcohol or other centrally acting sedatives should be avoided. Although Pseudoephedrine has no pressor effects in normotensive patients but Pseudoephedrine, guaiphenasine & triprolidine should be used with caution to patients suffering from mild to moderate hypertension. Moreover, caution should also be exercised in the following disease conditions - hypertension and heart disease, diabetes, hyperthyroidism, elevated intra-ocular pressure, prostatic enlargement, severe renal and hepatic impairment. This preparation should not be used for persistent or chronic cough, which occurs with smoking, asth..

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Aristovit M Tablet 30's pack

Aristovit M Tablet 30's pack

Aristovit® M is sugar-coated multivitamin mineral tablet. Aristovit® -M is indicated in deficiency states in acute and chronic disease. Conditions regarding specific support: pregnancy, lactation, menopause, during treatment with antibiotics. The comprehensive formulae of Aristovit® M assures liberal amounts of important vitamins, minerals and trace elements needed by the body during periods of increased energy requirements such as in disease and convalescence.Provides 11 vitamins, 5 minerals & Iron in a single dose formulationTime-tested multivitamin & mineral brandSophisticated technology is utilized to produce the highest quality productProvides vitamin & mineral supplementation at an affordable costMeets the US recommended daily allowances (RDA) of vitamins & minerals..

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Bexipred Eye drop

Bexipred Eye drop

What Bexipred® is and what it is used for?Bexipred® is the preparation of prednisolone acetate which is belongs to a group of medicines known as steroidal anti-inflammatory drugs. Bexipred® is used in adults for the short-term treatment of eye inflammation.It reduces the irritation, burning, redness and swelling of eye inflammation caused by chemicals, heat, radiation, allergy, or foreign objects in the eye.Before you take Bexipred®Do not take this medicine and tell your doctor if:If you are allergic to prednisolone acetate, benzalkonium chloride or any of the other ingredients of this medicineIf you suffer from viral, fungal or bacterial eye infectionsIf you suffer from tuberculosis of the eyeIf you have injuries to or ulcers on the corneaIf you have previously had herpes simplexTake special care with Bexipred®Check with your doctor before taking this medicine if you suffer from, or have in the past suffered from:Eye ulcers or have had a disease or treatment to the eye that caused the tissue to become thinYou have glaucoma or are being treated for raised pressure within the eyeYou have had surgery for cataractsBacterial, viral or fungal eye infectionsTaking other medicinesTell your doctor if you are using or have used other steroid eye drops, as frequent or long-term use of steroids can result in additional side effects. Tell your doctor or pharmacist if you are using, have recently used or might use any other medicine, including medicines obtained without a prescription.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.How to take Bexipred® (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?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.The recommended dose is 1 or 2 drops into the affected eye(s) 2 to 4 times a day. During the first two days of treatment you may be asked to apply the drops as often as every hour.If you take more Bexipred® than you shouldPutting too many drops in your eye(s) is unlikely to lead to unwanted side effects. If you have placed too many drops in your eye(s), wash your eye(s) with clean water. Apply your next dose at the normal time.If, by accident, anyone drinks this medicine, contact your doctor straight away.If you forget to take Bexipred®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 Bexipred®Bexipred® should be used as advised by your doctor. Do not stop using Bexipred® until your doctor has told you to. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.Possible side effectsLike all medicines, Bexipred® 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 leafletHow to store Bexipred®?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...

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Bexitrol F HFA 25/125

Bexitrol F HFA 25/125

1. What Bexitrol® F is and what it is used for?Bexitrol® F metered dose inhaler is a combination of Salmeterol Xinafoate BP and Fluticasone Propionate BP. Salmeterol Xinafoate is a selective, long acting beta-2 agonist used in the treatment of asthma and other forms of diffuse airways obstruction. Fluticasone Propionate is a corticosteroid with mainly glucocorticoid activity. Fluticasone Propionate is stated to exert a topical effect on the lungs without systematic effects at usual dose.Bexitrol® F is indicated in the regular treatment of asthma where use of a combination product (long-acting beta-2-agonist and inhaled corticosteroid) is appropriate:patients not adequately controlled with inhaled corticosteroids and "as needed" inhaled short-acting beta-2-agonist orpatients already adequately controlled on both inhaled corticosteroids and long-acting beta-2-agonist2. Before you take Bexitrol® FBexitrol® F is contraindicated in patients with a history of hypersensitivity to any of the ingredients.Special Warnings and Special PrecautionsConsideration should be given to additional corticosteroid therapies, and to including administration of antibiotics if an infection is present. As with all inhaled medication containing corticosteroids, Bexitrol® F should be administered with caution in patients with active or quiescent pulmonary tuberculosis. Bexitrol® F should be administered with caution in patients with thyrotoxicosis.Precaution for Paediatric UseOrally inhaled corticosteroids may cause a reduction in growth velocity when administered to paediatric patients. The long-term effects of this reduction including the impact of final adult height are unknown.Administration of drugs during pregnancy and lactation should only be considered if the expected benefit to the mother is greater than any possible risk to the foetus or child.There are no data available for human breast milk.Taking other medicinesBoth non-selective and selective b-blockers should be avoided in patients with asthma, unless there are compelling reasons for their use. Due to the very low plasma concentrations achieved after inhaled dosing clinically significant drug interactions are unlikely. Care should be taken when co-administering known strong CYP3A4 inhibitors (e.g. ketoconazole, ritonavir), as there is potential for increased systemic exposure to Fluticasone Propionate.3. How to take Bexitrol® F?Adults and adolescents 12 years and older-Two inhalations of 25 mg Salmeterol and 50 mg Fluticasone Propionate twice daily. or,Two inhalations of 25 mg Salmeterol and 125 mg Fluticasone Propionate twice daily. or,Two inhalations of 25 mg Salmeterol and 250 mg Fluticasone Propionate twice daily.Important information for PatientsPrime your Bexitrol® F InhalerBexitrol® F inhaler should be primed before using it for the first time. You should also prime your inhaler when the inhaler has not been used for more than 14 days or when the inhaler has been dropped.To prime, simply shake the inhaler well and then spray 4 times into the air away from your face, shaking well before each spray.How to use your inhaler correctly?Remove the cap from the mouthpiece of the actuatorMake sure the mouthpiece is clean inside and outside.Hold the inhaler by placing your index finger on top of the metal canister and thumb on the bottom of the plastic mouthpiece. Shake it well.Raise the Inhaler to your mouth. Put the mouthpiece between your teeth, but do not bite it. Close your lips around the mouthpiece. Breathe out slowly and gently through the Inhaler until your lungs feel comfortably empty.Tilt your head back slightly. Start to breathe in slowly through your mouth. As you start to breathe in, press down firmly on the top of the can to release your medicine continue to breathe in steadily and deeply.Hold your breath. Remove the inhaler from your mouth. Continue to hold your breath as long as possible, up to 10 seconds. Then breathe out gently. If you are taking a second puff, wait about one minute, then repeat steps 3 to 6.Replace the mouthpiece cap after each useA handy tip for ChildrenChildren and others who have weaker hands may have difficulty pressing down on the top of the can with just one hand. They can use both hands to make their Inhaler work.Cleaning your InhalerKeeping the plastic actuator clean is very important to prevent medicine buildup and blockage. The actuator should be washed, shaken to remove excess water and air-dried thoroughly at least once a week. The inhaler may stop spraying if not properly cleaned.How to clean your Inhaler?Remove the metal canister from the plastic casing of the inhaler and remove the mouthpiece cover.Rinse the actuator thoroughly with warm water.Dry the actuator thoroughly inside and outside.Replace the metal canister and the mouthpiece cover.Do not put the metal canister in water.In case of emergency situation when you feel you are not relieved despite using your inhaler, y..

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Brodil hfa (Inhaler) 100mcg/puffs

Brodil hfa (Inhaler) 100mcg/puffs

Price৳ 194 TKNameBrodil HFAGenericsalbutamolTypeInhalerQuantity1's packDose100mcg/puffs..

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Famotack 40mg Tab

Famotack 40mg Tab

Indication:Duodenal ulcer, Gastric ulcer, Gastro-esophageal reflux disease and Zollinger-Ellison syndrome, Gastritis.Dosage & Administration:Tablet:20 mg twice daily. Maintenance therapy as Famotack® 20 one tablet at night.Powder for Suspension:Gastroesophageal Reflux Disease (GERD):< 1 year of age: 0.5 mg/kg/dose of famotidine oral suspension up to 8 weeks once daily in patientsAge 3 to 11 months: 0.5 mg/kg/dose twice daily up to 8 weeksAge 1 to 2 months: 0.5 mg/kg/dose once daily up to 8 weeksNeonates: 0.5 mg/kg/dose maximum once daily up to 8 weeksPatients 1-16 years of age:Gastroesophageal Reflux Disease (GERD):1.0 mg/kg/day p.o. divided b.i.d. up to 40 mg b.i.d.Duodonal ulcer: 0.5 mg/kg/day p.o. at bedtime or divided b.i.d. up to 40 mg/day.Peptic ulcer: 0.5 mg/kg/day p.o. at bedtime or divided b.i.d. up to 40 mg/day.Maintenance therapy: 40 mg at daily night.Reflux esophagitis: 2 mg/kg/dayZollinger- Ellison Syndrome: 40 mg 3 times daily.Preparation:Famotack® 20 tablet : Box containing 10 x 10 tablets in blister pack.Famotack® 40 tablet : Box containing 5 x 10 tablets in blister pack.Famotack Powder for suspension: Box containing sealed cap HDPE bottle containg dry powder for reconstituting 50 ml suspension with a dropper...

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FRABEX 500 Injection

FRABEX 500 Injection

Indication: 1. Haemorrhage or risk of haemorrhage in increased fibrinolysis or fibrinogenolysis like: Prostatectomy and bladder surgery, Menorrhagia, Epistaxis, Conisation of the cervix, Management of dental extraction in patients with coagulopathies,Ulcerative colitis, Haematuria,Gastrointestinal haemorrhage. 2. General fibrinolysis as in prostatic and pancreatic cancer, after thoracic and other major surgery, in obstetrical complications such as abruptio placentae and post-partum haemorrhage, in leukaemia and liver diseases and in connection with thrombolytic therapy with streptokinase. 3. Hereditary angioneurotic oedema.Dosage & Administration:Prostatectomy: 5-10 ml by slow IV injection every eight hours for the first 3 days after surgery; thereafter 1-1.5 gm orally 3-4 times daily; Menorrhagia: 1-1.5 gm orally 3-4 times daily for 3-4 days; EPISTAXIS: 1.5 gm orally 03 times daily for 4-10 days; Haematuria: 1-1.5g orally 2-3 times daily; Conisation of the Cervix: 1.5 gm orally 3 times daily for 12-14 days post-operatively; Dental Surgery in Patients with Coagulopathies: Immediately before surgery, 10 mg/kg body-weight should be given intravenously. After surgery, 25 mg/kg body-weight is to given orally 3-4 times daily for 6-8 days; General Fibrinolysis: 1 gm by slow IV injection 3-4 times daily; Hereditary Angioneurotic Oedema: 1-1.5 gm orally 2-3 times daily. (For detail please see the full prescribing information)..

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GERMISOL 50ml Hand Rub

GERMISOL 50ml Hand Rub

Indication: For the disinfection of clean and intact skin. For pre-operative surgical hand disinfection, hand disinfection on the ward prior to aseptic procedures or after handling contaminated materials. For disinfection of the patients' skin prior to surgery or other invasive procedures.Dosage & Administration:For external use only. Adults: Pre-operative surgical hand disinfection: Dispense 5 ml of solution and spread thoroughly over both hands and forearms, rubbing vigorously. When dry apply a further 5 ml and repeat the procedure. Antiseptic hand disinfection on the ward: Dispense 3 ml of solution and spread thoroughly over the hands and wrists rubbing vigorously until dry. Disinfection of patients' skin: Prior to surgery apply the solution to a sterile swab and rub vigorously over the operation site for a minimum of 2 minutes. Chlorhexidine Gluconate is also used for preparation of the skin prior to invasive procedures such as venepuncture. Elderly and children: There are no special dosing regimens for children and the elderly. ..

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KOP IM100mg Injection

KOP IM100mg Injection

Indication: Ankylosing spondylitis, osteoarthritis, and rheumatoid arthritis, bursitis and tendinitis, dysmenorrhoea or postoperative pain and acute gout or soft-tissue disorders.Dosage & Administration:SR Capsule: 100-200 mg once daily...

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LORATIN suspension

LORATIN suspension

Indication: Allergic rhinitis, Skin allergies including Chronic Idiopathic Urticaria (CIU).Dosage & Administration:Adult and child over 6 years: One Loratin® 10 mg tablet or two teaspoonful (10 ml) Loratin® suspension once daily. Children aged 2-5 years: 5 ml or 1 teaspoonful (5 mg) suspension once daily. Loratadine is not recommended for children under 2 years of age...

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Neodrop Pediatric Drops

Neodrop Pediatric Drops

Neodrop® Paediatric Drops is an antiflatulent and anticolic containing simethicone. Simethicone USP contains 4 to 7% w/w of silicon dioxide. Each ml drop contains 67 mg simethicone USP. Neodrop® (simethicone) is used as an antiflatulent to relieve symptoms commonly referred to gas including upper GI bloating, pressure, fullness or stuffed feeling. It is indicated in Flatulence, abdominal distention, fullness, gas and windy colic. Neodrop® can also be used prior to gastroscopy to enhance visualization and prior to radiography of the intestine to reduce gas shadows.Fast and effective relief from infant colicFDA approved most common OTC product in developed countriesAlcohol free highly palatable orange flavored drops Neodrop Prescribing InformationLocated in: Gastrointestinal..

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Ofran 8 mg/4 ml IV Injection

Ofran 8 mg/4 ml IV Injection

Indication:1. Prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy.2. Prevention of nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy.3. Prevention of nausea and vomiting associated with radiotherapy4. Prevention of postoperative nausea and/or vomitingDosage & Administration:1. Chemotherapy induced nausea & vomiting (CINV): Adult- For highly emetogenic chemotherapy recommended adult oral dosage of Ofran® is 24 mg given as three 8 mg tablets. For moderately emetogenic chemotherapy the oral dose is one 8mg Ofran® (Ondansetron) tablet or 10 ml of Ofran® oral solution twice daily Pediatric patients- for pediatric patients from 4 to 11 years of age the dosage is one 4mg Ofran® tablet or 5ml of Ofran® solution 3 times per day for 1 to 2 days after completion of chemotherapy.2. Radiotherapy induced nausea and vomiting (RINV): Adult- the recommended oral dosage is one 8-mg Ofran® tablet or 10 mL of Ofran® Oral Solution given 3 times a day.3. Post-operative nausea & vomiting (PONV): Adult- the recommended dosage is 16 mg given as two 8 mg Ofran® tablets or 20 ml of Ofran® oral solution 1 hour before induction of anesthesia.Preparation:Ofran® 8 mg Tablet: Each box contains 30 tablets in blister packOfran® Oral Solution: Each bottle contains 50 ml oral solutionOfran® 8 mg IV Injection: Each box contains 6 ampoules in blister pack..

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PENVIK 100ml Dry Syrup

PENVIK 100ml Dry Syrup

Indication:Streptococcal infections, scarlet fever, mild erysipelas, Bacterial endocarditis, lobar pneumonia.Dosage & Administration:250 to 500 mg 6 hourlyPreparation:Penvik® Tablet :Each box containing 10x10 tablets in strip pack.Penvik® DS Tablet :Each box containing 10x10 tablets in strip pack.Penvik® Forte Dry Syrup : Each bottle containing dry powder to make 100ml syrup and a measuring spoon...

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Phylopen Powder for Suspension 100 ml bottle

Phylopen Powder for Suspension 100 ml bottle

Indication:Boils, abscesses, carbuncles, furunculosis, cellulitis; infected skin conditions, e.g. ulcer, eczema and acne; infected. wounds, infected burns, protection for skin grafts, otitis media and externa, impetigo, pneumonia, lung abscess, empyema, sinusitis, pharyngitis, tonsillitis, and quinsy, osteomyelitis, enteritis, endocarditis, urinary tract infections, meningitis, septicaemia, prophylactic agent during major surgical procedures for example, cardiothoracic and orthopaedic surgery.Dosage & Administration:500 mg six hourly, 2-10 years : half of the adult dose, Under 2 years : quarter of the adult dose.Preparation:Phylopen® 250 capsule : Box containing 100 capsules in strip pack.Phylopen® DS capsule : Box containing 42 capsules in alu-alu blister pack.Phylopen® Powder for Suspension : Bottle containing dry powder for reconstitution to 100 ml syrup.Phylopen® Forte Powder for Suspension : Bottle containing dry powder for reconstitution to 100 ml syrup.Phylopen® 500 injection: Box containing 5 blister packs, each containing one vial of Phylopen® 500 injection and one 5 ml ampoule of Water for Injection...

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Pylotrip R Tablet 7's pack

Pylotrip R Tablet 7's pack

ndication: Pylotrip® R is indicated for the eradication of H. pylori in active chronic gastric, duodenal and gastric ulcers. Dosage & Administration:Each Pylotrip® R strip twice daily for 7-14 days or as per the physician's advice. ..

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Repres plus 2 Tablet

Repres plus 2 Tablet

Indication: Essential hypertension. Dosage & Administration:One tablet daily, preferably to be taken in the morning and before a meal...

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Savlon  antiseptic 1000ml

Savlon antiseptic 1000ml

With Savlon Disinfectant Liquid's powerful antibacterial formula, however, you can make sure your family are protected. Use it on worktops, sinks, chopping boards, high chairs, changing mats, tables, toilets, showers, playrooms? anywhere around the house...

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Savlon antiseptic cream 60g

Savlon antiseptic cream 60g

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Savlon Antiseptic Liquid 112ml

Savlon Antiseptic Liquid 112ml

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SONAP 15 gm Gel

SONAP 15 gm Gel

Indication: Rheumatoid arthritis, degenerative arthritis, ankylosing spondylitis, juvenile rheumatoid arthritis, tendinitis, bursitis, acute gout, acute musculoskeletal disorders (such as sprains, direct trauma and fibrositis), migraine and dysmenorrhoea.Dosage & Administration:Tablet & Suppository - Rheumatoid arthritis, osteoarthritis, ankylosing spondylitis: 250 to 500 mg twice daily. May be increased to 1.50 gm for limiting periods. Mild to moderate pain, primary dysmenorrhoea, acute tendinitis, bursitis, and dysmenorrhoea: 500 mg initially, followed by every 250 mg every 6 to 8 hours as required. Do not exceed a 1.375 gm total daily dose. Acute gout: 750 mg, then 250 mg every6 8 hours until attack subsides. Juvenile arthritis (Children over 5 years): 10 gm/kg daily in two divided doses is recommended. Gel - Is to be applied 2 - 6 times a day as required and is not recommended for use in children...

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Sonap 500mg Suppo 10's pack

Sonap 500mg Suppo 10's pack

Indication: Rheumatoid arthritis, degenerative arthritis, ankylosing spondylitis, juvenile rheumatoid arthritis, tendinitis, bursitis, acute gout, acute musculoskeletal disorders (such as sprains, direct trauma and fibrositis), migraine and dysmenorrhoea.Dosage & Administration:Tablet & Suppository - Rheumatoid arthritis, osteoarthritis, ankylosing spondylitis: 250 to 500 mg twice daily. May be increased to 1.50 gm for limiting periods. Mild to moderate pain, primary dysmenorrhoea, acute tendinitis, bursitis, and dysmenorrhoea: 500 mg initially, followed by every 250 mg every 6 to 8 hours as required. Do not exceed a 1.375 gm total daily dose. Acute gout: 750 mg, then 250 mg every6 8 hours until attack subsides. Juvenile arthritis (Children over 5 years): 10 gm/kg daily in two divided doses is recommended. Gel - Is to be applied 2 - 6 times a day as required and is not recommended for use in children...

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Ex Tax: Tk.120.50/=

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