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Adiponil Capsule

Adiponil Capsule

IndicationsAdiponil is indicated for long term treatment of significantly obese patients, including patients with risk factors associated with obesity, in conjunction with a mildly hypocaloric diet. Adiponil is also indicated in long term weight control such as weight loss, weight maintenance and prevention of weight regainDescriptionsAdiponil is a potent, specific and reversible long acting inhibitor of gastrointestinal lipases for obesity management that acts by inhibiting the absorption of dietary fat. It exerts its therapeutic activity in the human stomach and small intestine by forming a covalent bond with the active serine residue of the active site of gastric and pancreatic lipases. The inactivated enzymes are thus unable to hydrolyze the dietary fat in the form of triglycerides, into absorbable free fatty acids and monoglycerides. As undigested triglycerides are not absorbed, the resulting calorie deficit has a positive effect on weight control. Systemic absorption of the drug is therefore not needed for activity. At the recommended therapeutic dose of 120 mg three times a day, Orlistat inhibits dietary fat absorption by approximately 30 %.Dosage & AdministrationThe recommended dose of Adiponil is one 120 mg capsule three times a day with each main meal (during or upto 1 hour after the meal).Side EffectsGenerally Adiponil is well tolerated. However few side effects including oily spotting, flattus with discharge, faecal urgeney, oily evaculation, increased defaecation may be seen after administration of orlistatPrecautionsPatients should be advised to adhere to dietary guidelines. gastrointestinal events may increase when orlistat is taken with a diet high in fat (>30% of calories from fat). The daily intake of fat should be distributed over three main meals. If a meal is missed, the dose of orlistat may be omitted.ContraindicationsOrlistat is contraindicated in patients with chronic malabsorption syndrome, cholestasis and in patients with known hypersensitivity to orlistat or to any components of this product.Use in Pregnancy & LactationThere are no adequate and well controlled studies of orlistat in pregnant women. Orlistat is not recommended for use during pregnancy. It is not known if orlistat is secreted in human breast milk. Orlistat should not be taken by nursing women.OverdoseSingle doses of 800 mg and multiple doses of up to 400 mg three times a day for 15 days have been studied in normal weight and obese subjects without significant adverse findings. If a significant overdose of orlistat occur, it is recommended that the patient be observed for 24 hours. Based on human and animal studies, any systemic effects attributable to the lipase inhibiting properties of orlistat should be rapidly reversibleCommercial PackagingAdiponil capsule: Each box contains 1 blister strip of 10 capsules..

Tk.40.00/=

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Adora 1000 Tablet

Adora 1000 Tablet

Adora..

Tk.32.00/=

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Adora 500 Capsule

Adora 500 Capsule

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. ..

Tk.18.00/=

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Adora Suspension

Adora Suspension

Adora DS..

Tk.60.00/=

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Adora Suspension  100 ml

Adora Suspension 100 ml

Adora Susp..

Tk.90.00/=

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Adrinor 1mg 1 ml Injection

Adrinor 1mg 1 ml Injection

IndicationsAdjunctive use in the management of cardiac arrest. It is used in cardiopulmonary resuscitation. Intracardiac puncture and intramyocardial injection of adrenaline may be effective when external cardiac compression and attempts to restore the circulation by electrical defibrillation or use of a pacemaker fail. Adrenaline is a drug that leads to increased blood pressure, increased heart rate, increased air entry, increased blood glucose, stimulates cardiac activity and reduces allergic reactions by reducing inflammatory response caused by histamine. Due to these properties, it is used for the treatment of allergic and anaphylactic reactions. Adrenaline is the favored treatment for anaphylactic shock and should be administered immediately if a person begins exhibiting severe allergic reactions. Adrenaline is also used in life threatening asthma when failing ventilation and continued deterioration despite nebulizer therapy.DescriptionsAdrenaline is a direct-acting sympathomimetic agent exerting its effect on alpha and beta-adrenoceptors. The overall effect of adrenaline depends on the dose, and may be complicated by the homeostatic reflex responses. In resuscitation procedures it is used to increase the efficacy of basic life support. It is a positive cardiac inotrope. Major effects are increased systolic blood pressure by arterioral and venous vasoconstriction (alpha1 effects), reduced diastolic pressure, tachycardia and hyperglycaemia. Adrenaline is rapid in onset and with short duration. After IV infusion the half-life is approximately 5-10 minutes. It is rapidly distributed to the heart, spleen, several glandular tissues and adrenergic nerves. Adrenaline is rapidly metabolised in the liver and tissues by oxidative de-amination and O-methylation followed by reduction or by conjugation with glucuronic acid or sulphate. Up to 90% of the IV dose is excreted in the urine as metabolites. It is approximately 50% bound to plasma proteins.Dosage & AdministrationCardiac arrest: 1. Intravenous injection: 1 mg injection repeated every 2-3 minutes as necessary. 2. Endotracheal: 2-3 mg via an endotracheal tube, repeated as necessary. 3. Intracardiac injection: 0.1 to 1 mg, direct into the atrium of the heart. 4. Intraspinal use: Usual dose is 0.2 to 0.4 mg added to anesthetic spinal fluid mixture (to prolong anesthetic action by limiting absorption). Anaphylaxis, asthma or severe bronchospasm: Adult dose is 0.25 - 0.5 mg. It may be repeated at 5 minutes intervals until perfusion and respiratory status normalizes. In case of dose dilution: 1 mg of Adrenaline to be diluted in 9 ml Normal Saline. Children: Intravenous injection: Initially 10 mcg/kg body weight, not to exceed 250 mcg. May be repeated every 3-5 minutes if necessary. Subsequent doses should be 100 mcg/kg.Side EffectsAnxiety, restlessness, dizziness, headache, palpitations, rapid pulse, tremors, weakness and coldness of the extremities may be reported even with small doses and especially when given in conjunction with local anaesthetics.PrecautionsThe solution should not be used if it is pinkish or darker than slightly yellow or if it contains a precipitate. Adrenaline is readily destroyed by alkalies and oxidizing agents. In the latter category are Oxygen, Chlorine, Iodine, Permanganates, Chromates, Nitrites and salts of easily reducible metals, especially Iron. Adrenaline should not be mixed with Sodium bicarbonate; the solution is oxidised to adrenochrome and then forms polymers. Special warnings and precautions for use Administer slowly with caution to elderly patients and to patients with ischemic heart disease, hypertension, diabetes mellitus, hyperthyroidism or psychoneurosis. Use with extreme caution in patients with long-standing bronchial asthma and emphysema who have developed degenerative heart disease. Anginal pain may be induced when coronary insufficiency is present.ContraindicationsHypertension, arteriosclerosis, coronary disease and hyperthyroidism. Not to be given to patients taking monoamine oxidase inhibitors.Use in Pregnancy & LactationPregnancy Category C. It crosses the placenta and is excreted in breast milk. Adrenaline should only be used in pregnancy if the potential benefits outweigh the risks to the fetus. Lactating mothers: It is excreted in breast milk and therefore Adrenaline is not recommended for use during lactation because of the risk of adverse effects of infants.Drug InteractionUse of Adrenaline with excessive doses of digitalis, mercurial diuretics or other drugs that sensitize the heart to arrhythmias is not recommended. The adverse effects of Adrenaline may be potentiated by tricyclic antidepressants; certain antihistamines; e.g, Diphenhydramine, Tripelennamine, Chlorpheniramine and L-thyroxine Sodium.OverdoseSymptoms: Cardiac arrhythmia leading to ventricular fibrillation, severe hypertension leading to pulmonary edema and cerebral hemorrhage. Treatmen..

Tk.25.00/=

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Alestor Tab

Alestor Tab

Alestor Tab..

Tk.8.00/=

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Algicid suspension

Algicid suspension

IndicationsTreatment of symptoms of gastro-oesophageal reflux, such as acid regurgitation, heartburn and indigestion (related to reflux), for example, following meals or during pregnancy or in patients with symptoms related to reflux esophagitis.DescriptionsAlgicid works by forming a raft (thick layer) on top of the stomach contents soon after it has made contact with the stomach acid. The raft acts as a strong physical barrier and helps keep all the components of the stomach contents in the stomach where they work, not letting them seep back up into the esophagus where they hurt.Dosage & AdministrationDaily 4 times, after meals & before bedtime. Tablet Adult and child over 12 years: 1-2 tablets. Child 6-12 years: 1 tablet. Suspension Adult and child over 12 years: 5-10 ml. Child 2-12 years: 2.5-5 ml. Algicid is not recommended for children under 2 years of age.Side EffectsIn addition to the desired effect of the drug, some side effects may appear such as: nausea, constipation, diarrhea or headache. In these cases consult a physician. In case too big dosage has been taken, there might appear a sensation of swelling. In this case it is advisable to consult a physician.PrecautionsAlgicid should be prescribed with caution in patients with renal impairment and congestive cardiac failure.ContraindicationsSodium alginate and potassium bicarbonate is contraindicated in patients with known hypersensitivity to these.Use in Pregnancy & LactationAlgicid can be given in pregnant and lactating women.Drug InteractionIf you are taking other medicines concomitantly, or have just completed another drug treatment, inform your physician in order to prevent hazards or inefficacy arising from drug interactions.OverdoseOver dosage with this formulation is a rare case. In case of overdose please consult with a registered physician.StorageStore in a cool place (in room temperature, below 30 °C).Commercial PackagingAlgicid tablet: Each box contains 10 blisters of 10 tablets. Algicid suspension: Bottle containing 200 ml of suspension...

Tk.150.00/=

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Algicid Tablet

Algicid Tablet

IndicationsTreatment of symptoms of gastro-oesophageal reflux, such as acid regurgitation, heartburn and indigestion (related to reflux), for example, following meals or during pregnancy or in patients with symptoms related to reflux esophagitis.DescriptionsAlgicid works by forming a raft (thick layer) on top of the stomach contents soon after it has made contact with the stomach acid. The raft acts as a strong physical barrier and helps keep all the components of the stomach contents in the stomach where they work, not letting them seep back up into the esophagus where they hurt.Dosage & AdministrationDaily 4 times, after meals & before bedtime. Tablet Adult and child over 12 years: 1-2 tablets. Child 6-12 years: 1 tablet. Suspension Adult and child over 12 years: 5-10 ml. Child 2-12 years: 2.5-5 ml. Algicid is not recommended for children under 2 years of age.Side EffectsIn addition to the desired effect of the drug, some side effects may appear such as: nausea, constipation, diarrhea or headache. In these cases consult a physician. In case too big dosage has been taken, there might appear a sensation of swelling. In this case it is advisable to consult a physician.PrecautionsAlgicid should be prescribed with caution in patients with renal impairment and congestive cardiac failure.ContraindicationsSodium alginate and potassium bicarbonate is contraindicated in patients with known hypersensitivity to these.Use in Pregnancy & LactationAlgicid can be given in pregnant and lactating women.Drug InteractionIf you are taking other medicines concomitantly, or have just completed another drug treatment, inform your physician in order to prevent hazards or inefficacy arising from drug interactions.OverdoseOver dosage with this formulation is a rare case. In case of overdose please consult with a registered physician.StorageStore in a cool place (in room temperature, below 30 °C).Commercial PackagingAlgicid tablet: Each box contains 10 blisters of 10 tablets. Algicid suspension: Bottle containing 200 ml of suspension...

Tk.3.50/=

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Alneed Capsule

Alneed Capsule

IndicationsAlneed is indicated for the treatment and prophylaxis of Iron, Folic acid, B-vitamins and Vitamin-C deficiency, especially during pregnancy and lactation.DescriptionsAlneed is a special preparation of Iron, Folic acid, B-vitamins and Vitamin-C.Dosage & AdministrationOne capsule daily. In more severe cases, 2 capsules a day may be required or as directed by the physician.Side EffectsGenerally well tolerated. However, a few allergic reactions may be seen.PrecautionsCare should be taken in patients who may develop iron overload, such as those with hemochromatosis, haemolytic anaemia or red cell aplasia. Iron chelates with tetracycline and absorption may be impaired.ContraindicationsThis product is contraindicated in patients with a known hypersensitivity to any of the ingredients.OverdoseAccidental overdose of iron containing products is a leading cause of fatal poisoning in children fewer than 6. Avoid higher doses if you have liver disease or hemochromatosis; excess can cause bloody diarrhea, vomiting, acidosis, darkened stools, abdominal pain. Symptoms may clear in a few hours. Riboflavin is reported to be completely safe and no toxic symptoms have been reported so far. Higher doses of Nicotinamide may cause vomiting, diarrhea. Sensory neuropathy was observed in individuals consuming more than 200 mg Pyridoxine for very long periods. No cases of Folic acid overdosages have been reported. Acute ingestion of Ascorbic acid, even of massive doses, is unlikely to cause significant effects.StorageStore in a dry place below 25 °C. Protect from light.Commercial PackagingAlneed : Each box contains 10 blister strips of 10's capsule...

Tk.3.00/=

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Alneed Gold

Alneed Gold

IndicationsAlneed Gold is indicated for the treatment and prophylaxis of Zinc, Iron, Folic Acid, B-vitamins deficiency especially during pregnancy and lactation.DescriptionsAlneed Gold is a special preparation of Iron Polymaltose Complex, Folic Acid, Zinc, and B-vitamins. Iron Polymaltose Complex is a water soluble, macromolecular complex of poly nuclear iron (III) hydroxide and partially hydrolysed dextrin ( Polymaltose). It does not interact with the food components and other medications and so there is no decrease in bioavailability of Iron Polymaltose Complex. This makes sure that with the consumption of this complex, iron gets utilized at a faster rate in the haemoglobin synthesis. Folic acid prevents neural tube defects. Zinc is essential for many metabolic processes, blood formation, wound healing and for immune system. Thiamine is essential for the functioning of the nervous and digestive systems. Riboflavin is important for digestion, immune system support and energy production. Pyridoxin is important for brain development, production of red blood cells, metabolism of proteins and to reduce morning sickness. Nicotinamide is important for energy, blood pressure and circulation. Dosage & AdministrationOne capsule daily. In more severe cases, 2 capsules a day may be required or as directed by the physician.Side EffectsGenerally well tolerated. However, a few allergic reactions may be seen.PrecautionsCare should be taken in patients who may develop iron overload, such as those with haemochromatosis, haemolytic anaemia or red cell aplasia. Iron chelates with tetracycline and absorption may be impaired.ContraindicationsThis product is contraindicated in patients with a known hypersensitivity to any of the ingredients.OverdoseAccidental overdose of iron containing products is a leading cause of fatal poisoning in children below 6 years. Avoid higher doses if you have liver disease or haemochromatosis; excess can cause bloody diarrhea, vomiting, acidosis, darkened stools, abdominal pain. Symptoms may clear in a few hours. Riboflavin is reported to be completely safe and no toxic symptoms have been reported so far. Higher doses of Nicotinamide may cause vomiting, diarrhea. Sensory neuropathy was observed in individuals consuming more than 200 mg Pyridoxine for very long periods. No case of Folic acid overdodage has been reported. Zinc toxicity has been seen in both acute and chronic forms. Ingestion of 150 to 450 mg of zinc per day have been associated with low copper status, altered iron function, reduced immune function, and reduced levels of high-density lipoproteins. So, Zinc at its RDA dosages dose not cause any significant effect.StorageStore in a dry place below 25 °C. Protect from light.Commercial PackagingAlneed Gold capsule: Each box contains 3 blister strips of 10 capsule...

Tk.6.00/=

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Alneed PLUS Cap

Alneed PLUS Cap

IndicationsAlneed Plus is indicated for the treatment and prophylaxis of Zinc, Iron, Folic Acid, B-vitamins and Vitamin-C deficiency especially during pregnancy and lactation.DescriptionsAlneed Plus is a special preparation of Zinc, Iron, Folic Acid, B-vitamins and Vitamin-C.Dosage & AdministrationOne capsule daily. In more severe cases, 2 capsules a day may be required or as directed by the physician.Side EffectsGenerally well tolerated. However, a few allergic reactions may be seen.PrecautionsCare should be taken in patients who may develop iron overload, such as those with haemochromatosis, haemolytic anaemia or red cell aplasia. Iron chelates with tetracycline and absorption may be impaired.ContraindicationsThis product is contraindicated in patients with a known hypersensitivity to any of the ingredients.OverdoseAccidental overdose of iron containing products is a leading cause of fatal poisoning in children below 6 years. Avoid higher doses if you have liver disease or haemochromatosis; excess can cause bloody diarrhea, vomiting, acidosis, darkened stools, abdominal pain. Symptoms may clear in a few hours. Riboflavin is reported to be completely safe and no toxic symptoms have been reported so far. Higher doses of Nicotinamide may cause vomiting, diarrhea. Sensory neuropathy was observed in individuals consuming more than 200 mg Pyridoxine for very long periods. No case of Folic acid overdodage has been reported. Acute ingestion of Ascorbic acid, even of massive doses, is unlikely to cause significant effects. Zinc toxicity has been seen in both acute and chronic forms. Ingestion of 150 to 450 mg of zinc per day have been associated with low copper status, altered iron function, reduced immune function, and reduced levels of high-density lipoproteins. So, Zinc at its RDA dosages dose not cause any significant effect.StorageStore in a dry place below 25 °C. Protect from light.Commercial PackagingAlneed Plus capsule: Each box contains 10 blister strips of 10 capsule. ..

Tk.3.50/=

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Aloxif Tab

Aloxif Tab

Aloxif Tab..

Tk.14.00/=

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Ambolyt Paediatric Drops

Ambolyt Paediatric Drops

Indications• Acute and chronic diseases of respiratory tracts associated with viscid mucus including acute and chronic bronchitis • Productive cough • Inflammatory diseases of Rhinopharyngeal tract (e.g. Laryngitis, Pharyngitis, Sinusitis and Rhinitis) associated with viscid mucus • Asthmatic bronchitis, Bronchial asthma with difficult departure of mucus • Bronchiectasis • Chronic pneumonia.DescriptionsAmbroxol is a metabolite of Bromhexine. It possesses mucokinetic (improvement in mucus transport) and secretolytic (liquefies secretions) properties. Ambroxol stimulates the serous cells of the glands of the mucous membrane of bronchi, increasing the content of mucus secretion. The mucolytic effect is associated with depolymerization and splitting of mucoproteins and mucopolysaccharide fibres, which leads to reduction in the viscosity of mucus. Expectoration of mucus is facilitated and breathing is eased considerably. Ambroxol stimulates production of phospholipids of surfactant by alveolar cells. Ambroxol has anti-inflammatory properties. In patients with COPD, it improves airway patency. Beside these, Ambroxol also exhibits anti-oxidant activity. Long-term use is possible because of the good tolerability of the preparation. Dosage & AdministrationAverage daily dose (preferably after meal). Ambolyt Paediatric Drops: 0-6 months 0.5 ml 2 times a day 6-12 months 1 ml 2 times a day 1-2 years 1.25 ml 2 times a day Ambolyt Syrup: 2-5 years 2.5 ml (1/2 teaspoonful) 2-3 times a day 5-10 years 5 ml (1 teaspoonful) 2-3 times a day 10 years and adults 10 ml (2 teaspoonful) 3 times a day.Side EffectsGastrointestinal side-effects like epigastric pain, gastric fullness may occur occasionally. Rarely allergic responses such as eruption, urticaria or angioneurotic edema may occur.PrecautionsAmbroxol should be given cautiously to patients with gastric and duodenal ulceration or convulsive disorders. Patients with hepatic and renal insufficiency should take it with caution.ContraindicationsContraindicated in known hypersensitivity to Ambroxol or Bromhexine.Use in Pregnancy & LactationPregnancy: Teratogenic and fetal toxicity studies have shown no harmful effect of Ambroxol. However, it is advised not to use during pregnancy, especially in the 1st trimester. Lactation: Safety during lactation has not been established.Drug InteractionAmbroxol has no interaction with cardioactive glycosides, corticosteroids, bronchodilators, diuretics and antibiotics (normally used in the treatment of bronchopulmonary affections). But Ambroxol should not be taken simultaneously with antitussives (e.g. Codeine) because mucus, which has been liquefied by Ambroxol, might not be expectorated.Commercial PackagingAmbolyt Syrup: Amber color bottle containing 100 ml syrup and a measuring cup. Ambolyt Paediatric Drops: Amber color bottle containing 15 ml paediatric drops and a calibrated dropper..

Tk.30.00/=

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Ambolyt Syrup

Ambolyt Syrup

Indications• Acute and chronic diseases of respiratory tracts associated with viscid mucus including acute and chronic bronchitis • Productive cough • Inflammatory diseases of Rhinopharyngeal tract (e.g. Laryngitis, Pharyngitis, Sinusitis and Rhinitis) associated with viscid mucus • Asthmatic bronchitis, Bronchial asthma with difficult departure of mucus • Bronchiectasis • Chronic pneumonia.DescriptionsAmbroxol is a metabolite of Bromhexine. It possesses mucokinetic (improvement in mucus transport) and secretolytic (liquefies secretions) properties. Ambroxol stimulates the serous cells of the glands of the mucous membrane of bronchi, increasing the content of mucus secretion. The mucolytic effect is associated with depolymerization and splitting of mucoproteins and mucopolysaccharide fibres, which leads to reduction in the viscosity of mucus. Expectoration of mucus is facilitated and breathing is eased considerably. Ambroxol stimulates production of phospholipids of surfactant by alveolar cells. Ambroxol has anti-inflammatory properties. In patients with COPD, it improves airway patency. Beside these, Ambroxol also exhibits anti-oxidant activity. Long-term use is possible because of the good tolerability of the preparation. Dosage & AdministrationAverage daily dose (preferably after meal). Ambolyt Paediatric Drops: 0-6 months 0.5 ml 2 times a day 6-12 months 1 ml 2 times a day 1-2 years 1.25 ml 2 times a day Ambolyt Syrup: 2-5 years 2.5 ml (1/2 teaspoonful) 2-3 times a day 5-10 years 5 ml (1 teaspoonful) 2-3 times a day 10 years and adults 10 ml (2 teaspoonful) 3 times a day.Side EffectsGastrointestinal side-effects like epigastric pain, gastric fullness may occur occasionally. Rarely allergic responses such as eruption, urticaria or angioneurotic edema may occur.PrecautionsAmbroxol should be given cautiously to patients with gastric and duodenal ulceration or convulsive disorders. Patients with hepatic and renal insufficiency should take it with caution.ContraindicationsContraindicated in known hypersensitivity to Ambroxol or Bromhexine.Use in Pregnancy & LactationPregnancy: Teratogenic and fetal toxicity studies have shown no harmful effect of Ambroxol. However, it is advised not to use during pregnancy, especially in the 1st trimester. Lactation: Safety during lactation has not been established.Drug InteractionAmbroxol has no interaction with cardioactive glycosides, corticosteroids, bronchodilators, diuretics and antibiotics (normally used in the treatment of bronchopulmonary affections). But Ambroxol should not be taken simultaneously with antitussives (e.g. Codeine) because mucus, which has been liquefied by Ambroxol, might not be expectorated.Commercial PackagingAmbolyt Syrup: Amber color bottle containing 100 ml syrup and a measuring cup. Ambolyt Paediatric Drops: Amber color bottle containing 15 ml paediatric drops and a calibrated dropper..

Tk.40.00/=

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Ameloss 5 Tab

Ameloss 5 Tab

Ameloss 5 Tab..

Tk.10.00/=

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Amidol 300 50 vial

Amidol 300 50 vial

IndicationsNEURORADIOLOGY-Lumber myelography, thoraco-cervical myelography, ANGIOGRAPHY- Cerebral angiography, selective coronary angiography, left ventriculography, aortography, angiocadiography, selective visceral arteriography, peripheral arteriography, digital subtraction angiography, venography, urography, OTHER DIAGNOSTIC PROCEDURES-Contrast enhancement in CT scanning, arthrography, fistulography.DescriptionsIopamidol, an organic Iodine compound and used as a non-ionic water soluble radiographic contrast medium. Iopamidol blocks X-rays as they pass through the body, thereby allowing body structures not containing Iodine to be visualized. The degree of opacity produced by Iopamidol is directly proportional to the total amount of the iodinated contrast agent in the path of the X-rays. The visualization of body structures is dependent upon the distribution and elimination of Iopamidol.Dosage & AdministrationAdult dosage NEURORADIOLOGY Lumber myelography: Amidol 300, 5-10 ml; Amidol 370, 6-13 ml Thoraco-cervical myelography: Amidol 300, 5-10 ml; Amidol 370, 6-13 ml ANGIOGRAPHY Cerebral angiography: Amidol 300, 5-10 ml; Amidol 370, 6-13 ml Selective coronary arteriography: Amidol 300/370, 4-8 ml/artery Peripheral arteriography: Amidol 300/370, 20-50 ml Venography: Amidol 300, 20-50 ml; Amidol 370, 24-60 ml Angiocardiography: Amidol 300/370, 30-80 ml Left ventriculography: Amidol 300/370, 30-80 ml Percutaneous transfemoral / renal arteriography: Amidol 300/370, 30 ml Selective renal arteriography: Amidol 300/370, 5-10 ml Selective visceral arteriography: Hepatic angiography: Amidol 300, 30 ml; Amidol 370, 70 ml Coeliac angiography: Amidol 300/370, 40-70 ml Superior mesenteric angiography: Amidol 300/370, 25-50 ml Inferior mesenteric angiography: Amidol 300/370, 5-30 ml Digital subtraction angiography: 30-50ml (10-20 ml/sec ) of Amidol 300/370,i.v 25 ml (left ventricle), 2-5 ml (coronary arteries) ,15 ml/sec. of Amidol 300/370 i.a for cardiac imaging UROGRAPHY Amidol 300/370, 40-80 ml i.v up to 1.5 ml/kg in severe renal disease. OTHER DIAGNOSTIC PROCEDURES Contrast enhancement in CT scanning: Amidol 300/370, 0.5-2.0 ml /kg Arthrography: Amidol 300, 1-10 ml Children: 1-2.5 ml/kg. Method of administration NEURORADIOLOGY Lumber myelography: A slow sub-arachnoid injection is made through a fine lumber puncture needle into one of the lower interspinous spaces (L3-L4 or L4-L5). Optimum contrast appears immediately after injections and films should be obtained promptly. Thoraco-cervical myelography: Following a slow sub-arachnoid injection the patient should be turned on his/her side and tilted 10o-20o head down under fluoroscopic control. In this manner it is possible to control movement of the contrast medium column into the dorsal region. If the cervical region is to be examined, the contrast medium should be run into the cervical region first, before the examination of the dorsal areas where it is progressively diluted. Amidol 300/370 may also be injected sub-occipitally or by lateral puncture technique .Care should be taken to ensure that the contrast medium does not move intracranially. It is generally recommended that in intrathecal use the patient should remain with a raised bed head and be kept well hydrated; following hydration it is preferable that the patient be allowed to be ambulatory . ANGIOGRAPHY Cerebral angiography: Any current technique is suitable for radiological visualization of the cerebral vasculature with Amidol 370/300 injection. Carotid and vertebral angiography, performed by catheterization or percutaneous injection techniques, require rapid injection which, if necessary, may be repeated. Peripheral arteriography and venography: Percutaneous injection into the appropriate blood vessel is used for visualization of peripheral arteries and veins. Angiocardiography, left ventriculography, selective coronary arteriography: Amidol 370/300 injection may be administered by rapid injection through a catheter into a suitable peripheral artery or vein. It can also be introduced under pressure through a cardiac catheter in to any of the heart chambers, or injected into large vessel for immediate visualization. The contrast medium may also be administered during selective catheterization of the coronary arteries. Aortography: The contrast medium may be introduced directly or by intra-arterial injection for visualization of the aorta and its main branches. Selective visceral angiography: Visualization can be achieved by selective catheterization and injection into the hepatic, coeliac or mesenteric arteries. Digital subtraction angiography: For cardiac imaging the contrast medium may be administered intra-arterially by selective catheterization to provide substrated images. Amidol 370/300 injected intravenously either centrally or peripherally is also recommended for use this modality. UROGRAPHY The contrast medium injected intravenously and rapid..

Tk.1,203.00/=

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Amidol 370 50 vial

Amidol 370 50 vial

IndicationsNEURORADIOLOGY-Lumber myelography, thoraco-cervical myelography, ANGIOGRAPHY- Cerebral angiography, selective coronary angiography, left ventriculography, aortography, angiocadiography, selective visceral arteriography, peripheral arteriography, digital subtraction angiography, venography, urography, OTHER DIAGNOSTIC PROCEDURES-Contrast enhancement in CT scanning, arthrography, fistulography.DescriptionsIopamidol, an organic Iodine compound and used as a non-ionic water soluble radiographic contrast medium. Iopamidol blocks X-rays as they pass through the body, thereby allowing body structures not containing Iodine to be visualized. The degree of opacity produced by Iopamidol is directly proportional to the total amount of the iodinated contrast agent in the path of the X-rays. The visualization of body structures is dependent upon the distribution and elimination of Iopamidol.Dosage & AdministrationAdult dosage NEURORADIOLOGY Lumber myelography: Amidol 300, 5-10 ml; Amidol 370, 6-13 ml Thoraco-cervical myelography: Amidol 300, 5-10 ml; Amidol 370, 6-13 ml ANGIOGRAPHY Cerebral angiography: Amidol 300, 5-10 ml; Amidol 370, 6-13 ml Selective coronary arteriography: Amidol 300/370, 4-8 ml/artery Peripheral arteriography: Amidol 300/370, 20-50 ml Venography: Amidol 300, 20-50 ml; Amidol 370, 24-60 ml Angiocardiography: Amidol 300/370, 30-80 ml Left ventriculography: Amidol 300/370, 30-80 ml Percutaneous transfemoral / renal arteriography: Amidol 300/370, 30 ml Selective renal arteriography: Amidol 300/370, 5-10 ml Selective visceral arteriography: Hepatic angiography: Amidol 300, 30 ml; Amidol 370, 70 ml Coeliac angiography: Amidol 300/370, 40-70 ml Superior mesenteric angiography: Amidol 300/370, 25-50 ml Inferior mesenteric angiography: Amidol 300/370, 5-30 ml Digital subtraction angiography: 30-50ml (10-20 ml/sec ) of Amidol 300/370,i.v 25 ml (left ventricle), 2-5 ml (coronary arteries) ,15 ml/sec. of Amidol 300/370 i.a for cardiac imaging UROGRAPHY Amidol 300/370, 40-80 ml i.v up to 1.5 ml/kg in severe renal disease. OTHER DIAGNOSTIC PROCEDURES Contrast enhancement in CT scanning: Amidol 300/370, 0.5-2.0 ml /kg Arthrography: Amidol 300, 1-10 ml Children: 1-2.5 ml/kg. Method of administration NEURORADIOLOGY Lumber myelography: A slow sub-arachnoid injection is made through a fine lumber puncture needle into one of the lower interspinous spaces (L3-L4 or L4-L5). Optimum contrast appears immediately after injections and films should be obtained promptly. Thoraco-cervical myelography: Following a slow sub-arachnoid injection the patient should be turned on his/her side and tilted 10o-20o head down under fluoroscopic control. In this manner it is possible to control movement of the contrast medium column into the dorsal region. If the cervical region is to be examined, the contrast medium should be run into the cervical region first, before the examination of the dorsal areas where it is progressively diluted. Amidol 300/370 may also be injected sub-occipitally or by lateral puncture technique .Care should be taken to ensure that the contrast medium does not move intracranially. It is generally recommended that in intrathecal use the patient should remain with a raised bed head and be kept well hydrated; following hydration it is preferable that the patient be allowed to be ambulatory . ANGIOGRAPHY Cerebral angiography: Any current technique is suitable for radiological visualization of the cerebral vasculature with Amidol 370/300 injection. Carotid and vertebral angiography, performed by catheterization or percutaneous injection techniques, require rapid injection which, if necessary, may be repeated. Peripheral arteriography and venography: Percutaneous injection into the appropriate blood vessel is used for visualization of peripheral arteries and veins. Angiocardiography, left ventriculography, selective coronary arteriography: Amidol 370/300 injection may be administered by rapid injection through a catheter into a suitable peripheral artery or vein. It can also be introduced under pressure through a cardiac catheter in to any of the heart chambers, or injected into large vessel for immediate visualization. The contrast medium may also be administered during selective catheterization of the coronary arteries. Aortography: The contrast medium may be introduced directly or by intra-arterial injection for visualization of the aorta and its main branches. Selective visceral angiography: Visualization can be achieved by selective catheterization and injection into the hepatic, coeliac or mesenteric arteries. Digital subtraction angiography: For cardiac imaging the contrast medium may be administered intra-arterially by selective catheterization to provide substrated images. Amidol 370/300 injected intravenously either centrally or peripherally is also recommended for use this modality. UROGRAPHY The contrast medium injected intravenously and rapid..

Tk.1,318.00/=

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Amikin 100 Inj

Amikin 100 Inj

Amikin 100 Inj..

Tk.160.00/=

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Amikin 500 Inj

Amikin 500 Inj

Amikin 500 Inj..

Tk.480.00/=

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Amlosartan 10/160 Tab

Amlosartan 10/160 Tab

Indications Amlodipine and Valsartan combination is indicated for the treatment of hypertension. This fixed combination drug is not indicated for the initial therapy of hypertension Therapeutic Class Combined antihypertensive preparations Pharmacology Amlodipine is a dihydropyridine calcium channel blocker that inhibits the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle. Valsartan blocks the vasoconstrictor and aldosterone-secreting effects of Angiotensin II by selectively blocking the binding of Angiotensin II to the AT1 receptor in many tissues, such as vascular smooth muscle and the adrenal gland. Its action is therefore independent of the pathways for Angiotensin II synthesis. Amlodipine and Valsartan have been shown to be effective in lowering blood pressure. Both Amlodipine and Valsartan lower blood pressure by reducing peripheral resistance, but calcium influx blockade and reduction of Angiotensin II vasoconstriction are complementary mechanisms. Dosage & Administration Amlodipine is an effective treatment of hypertension in once daily doses of 2.5 mg-10 mg while Valsartan is effective in doses of 80 mg-320 mg. In clinical trials with Amlodipine and Valsartan combination using Amlodipine doses of 5 mg-10 mg and Valsartan doses of 160 mg-320 mg, the antihypertensive effects increased with increasing doses. Interaction No drug interaction studies have been conducted with Amlodipine and Valsartan combination and other drugs, although studies have been conducted with the individual Amlodipine and Valsartan components Contraindications Amlodipine and Valsartan combination is contraindicated in patients who are hypersensitive to any compounds of this product. Side Effects The most common side effects include peripheral edema, vertigo, nasopharyngitis, upper respiratory tract infection and dizziness. Pregnancy & Lactation Pregnancy: Amlodipine and Valsartan combination should not be used in 2nd and 3rd trimester because it can cause fetal death .Nursing Mothers: It is not known whether Valsartan and Amlodipine are excreted in human milk. Because of the potential for adverse effects on the nursing infant, a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother. Precautions Amlosartan should be used with caution because there is a risk for fetal or neonatal morbidity, hypotension, myocardial infarction or increased angina.Dose should be titrated slowly in patients with impaired hepatic or severely impaired renal function. In general, calcium channel blockers should be used with caution in patients with heart failure. Overdose Effects Limited data of human overdosage have been reported. Use in Special Population Pediatric use: The safety and effectiveness has not been established in pediatric patients.Geriatric use: No differences in overall incidence of adverse events were observed in elderly.Renal impairment: No initial dosage adjustment is required for patients with mild or moderate renal impairment. Titrate slowly in patients with severe renal impairment. Hepatic impairment: No initial dosage adjustment is required for patients with mild or moderate liver insufficiency. Titrate slowly in patients with hepatic impairment. Storage Conditions Store in a cool dry place protected from light. Keep out of reach of children. ..

Tk.9.00/=

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Amlosartan 5/160 Tab

Amlosartan 5/160 Tab

Indications Amlodipine and Valsartan combination is indicated for the treatment of hypertension. This fixed combination drug is not indicated for the initial therapy of hypertension Therapeutic Class Combined antihypertensive preparations Pharmacology Amlodipine is a dihydropyridine calcium channel blocker that inhibits the transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle. Valsartan blocks the vasoconstrictor and aldosterone-secreting effects of Angiotensin II by selectively blocking the binding of Angiotensin II to the AT1 receptor in many tissues, such as vascular smooth muscle and the adrenal gland. Its action is therefore independent of the pathways for Angiotensin II synthesis. Amlodipine and Valsartan have been shown to be effective in lowering blood pressure. Both Amlodipine and Valsartan lower blood pressure by reducing peripheral resistance, but calcium influx blockade and reduction of Angiotensin II vasoconstriction are complementary mechanisms. Dosage & Administration Amlodipine is an effective treatment of hypertension in once daily doses of 2.5 mg-10 mg while Valsartan is effective in doses of 80 mg-320 mg. In clinical trials with Amlodipine and Valsartan combination using Amlodipine doses of 5 mg-10 mg and Valsartan doses of 160 mg-320 mg, the antihypertensive effects increased with increasing doses. Interaction No drug interaction studies have been conducted with Amlodipine and Valsartan combination and other drugs, although studies have been conducted with the individual Amlodipine and Valsartan components Contraindications Amlodipine and Valsartan combination is contraindicated in patients who are hypersensitive to any compounds of this product. Side Effects The most common side effects include peripheral edema, vertigo, nasopharyngitis, upper respiratory tract infection and dizziness. Pregnancy & Lactation Pregnancy: Amlodipine and Valsartan combination should not be used in 2nd and 3rd trimester because it can cause fetal death .Nursing Mothers: It is not known whether Valsartan and Amlodipine are excreted in human milk. Because of the potential for adverse effects on the nursing infant, a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother. Precautions Amlosartan should be used with caution because there is a risk for fetal or neonatal morbidity, hypotension, myocardial infarction or increased angina.Dose should be titrated slowly in patients with impaired hepatic or severely impaired renal function. In general, calcium channel blockers should be used with caution in patients with heart failure. Overdose Effects Limited data of human overdosage have been reported. Use in Special Population Pediatric use: The safety and effectiveness has not been established in pediatric patients.Geriatric use: No differences in overall incidence of adverse events were observed in elderly.Renal impairment: No initial dosage adjustment is required for patients with mild or moderate renal impairment. Titrate slowly in patients with severe renal impairment. Hepatic impairment: No initial dosage adjustment is required for patients with mild or moderate liver insufficiency. Titrate slowly in patients with hepatic impairment. Storage Conditions Store in a cool dry place protected from light. Keep out of reach of children. ..

Tk.8.00/=

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Amlosartan 5/80 Tab

Amlosartan 5/80 Tab

Amlosartan 5/80 Tab..

Tk.6.00/=

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Anacaine HC cream

Anacaine HC cream

Indications Hydrocortisone plus Lidocaine cream is used for the anti-inflammatory and anesthetic relief of itching, pain, soreness and discomfort due to hemorrhoids, anal fissures, pruritus ani and similar conditions of the anal area. Therapeutic Class Drugs used in Ano-rectal region Pharmacology Hydrocortisone is a corticosteroid used for its anti-inflammatory and immunosuppressive effects. Its anti-inflammatory action is due to the suppression of migration of polymorphonuclear leukocytes and reversal of increased capillary permeability. It may also be used as replacement therapy in adrenocortical insufficiency.Lidocaine is an amide type local anesthesia. It stabilises the neuronal membrane and inhibits Na ion movements, which are necessary for conduction of impulses. In the heart, lidocaine reduces depolarisation of the ventricles during diastole and automaticity in the His-Purkinje system. Duration of action potential and effective refractory period are also reduced. Dosage & Administration Apply twice daily around the anal opening in a thin layer using an applicator. Interaction This cream should be used with caution together with dental injection anaesthesia, other local anaesthetics or agents structurally related to local anaesthetics of amide type eg, antiarrhythmic drugs (eg, mexiletine), as the toxic effects of these drugs are additive.Patients treated with class III antiarrhythmic drugs (eg, amiodarone) should be closely observed and ECG monitoring should be considered, as the cardiac effects of lidocaine and class III antiarrhythmic drugs can be additive.Drugs that inhibit the metabolism of lidocaine (eg, cimetidine or ?-blockers) may cause potentially toxic plasma concentrations when lidocaine is given in repeated high doses over a long time period. Such interactions are of no clinical importance following short-term treatment with lidocaine at recommended doses. Contraindications Patients with a history of hypersensitivity to any of its ingredients. Side Effects Side effects like Rectal bleeding, Swelling of the skin, Adrenal suppression, Anaphylaxis, Angioedema, Cushing syndrome, Hirsutism, Acne, Cutaneous and subcutaneous atrophy, Dry scaly skin, Urticaria. Pregnancy & Lactation Pregnancy Category C. Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risksLactation: Unknown if distributed in breast milk; exercise caution Precautions If extensive areas are treated, the possibility of systemic absorption exists. Systemic absorption of topical steroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing's syndrome, hyperglycemia, and glycosuria in some patients. If irritation or sensitivity occurs or infection appears, discontinue use and institute appropriate therapy. ..

Tk.100.00/=

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Aprima 10mg Tablet

Aprima 10mg Tablet

Indications Apremilast is indicated for the treatment of adult patients with active psoriatic arthritis and moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy. Therapeutic Class Disease-modifying antirheumatic drugs (DMARDs) Pharmacology Apremilast is a novel, orally available small molecule inhibitor of type-4 cyclic nucleotide phosphodiesterase (PDE-4). PDE-4 is a cyclic adenosine monophosphate (cAMP)-specific phosphodiesterase that is predominantly located in inflammatory cells. By inhibiting PDE-4, apremilast increases intracellular levels of cAMP and thereby inhibits the production of multiple proinflammatory mediators including PDE-4, TNF-alpha, interleukin-2 (IL-2), interferon-gamma, leukotrienes, and nitric oxide synthase. By targeting a central component of the inflammatory signaling cascade rather than a single inflammatory marker, PDE-4 inhibition may restore the homeostatic balance between pro- and anti-inflammatory signalling. Dosage & Administration The recommended initial dosage titration of Apremilast from Day 1 to Day 5 is shown below. Following the 5-day titration, the recommended maintenance dosage is 30 mg twice daily taken orally starting on Day 6. This titration is intended to reduce the gastrointestinal symptoms associated with initial therapy. Apremilast can be administered without regard to meals.Day 1: 10 mg in morningDay 2: 10 mg in morning and 10 mg in evening Day 3: 10 mg in morning and 20 mg in evening Day 4: 20 mg in morning and 20 mg in evening Day 5: 20 mg in morning and 30 mg in evening Day 6: 30 mg twice dailyDosage adjustment in patients with severe renal impairment. Apremilast dosage should be reduced to 30 mg once daily in patients with severe renal impairment. For initial dosage titration, it is recommended that Apremilast be titrated using only the morning schedule and the evening doses be skipped. Interaction Co-administration of strong cytochrome P450 enzyme inducer Rifampin resulted in a reduction of systemic exposure of Apremilast.Therefore.the use of cytochrome P450 enzyme inducers (e.g. Rifampin, Phenobarbital,Carbamazepine, Phenytoin) with Apremilast is not recommended. Contraindications Apremilast is contraindicated in patients with a known hypersensitivity to Apremilast or to any of the excipients in the formulation. Side Effects The most frequently occurring side effects of Apremilast are nausea, diarrhea and headache. Other less frequent side effects are upper respiratory tract infection, vomiting, naospharyngitis, abdominal pain, hypersensitivity, gastroesophageal reflux disease, dyspepsia, fatigue, decrease appetite, cough, rash, insomnia. Pregnancy & Lactation Pregnancy Category C. It is not known whether Apremilast or its metabolites are present in human milk; however, Apremilast was detected in milk of lactating mice. Caution should be exercised when Apremilast is administered to a nursing woman. Precautions Treatment with Apremilast is associated with an increase in adverse reactions of depression. Patients, their caregivers and families should be advised of the need to be alert for the emergence or worsening of depression, suicidal thoughts or other mood changes and if such changes occur to contact their healthcare provider. Prescribers should carefully evaluate the risks and benefits of continuing treatment with Apremilast if such events occur.During the controlled period of the studies in psoriatic arthritis, weight decrease between 5-10% of body weight was reported in 10% of subjects treated with Apremilast 30 mg twice daily compared to 3.3% treated with placebo. Use in Special Population Use in Paediatric patient: The safety and effectiveness of Apremilast in paediatric patients less than 18 years of age have not been established. ..

Tk.25.00/=

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Aqualax powder for solution.

Aqualax powder for solution.

Indications Polyethylene Glycol is indicated in the treatment of constipation. This should be used for 2 weeks or less or as directed by physician. Polyethylene Glycol 3350 is a prescription only laxative that has been prescribed by physician to treat constipation. This product should only be used by the person for whom it is prescribed. Therapeutic Class Osmotic purgatives Description This is white powder for reconstitution. It is a synthetic polyglycol having an average molecular weight of 3350. Polyethylene Glycol is an osmotic agent that causes water to be retained with the stool. Polyethylene Glycol appears to have no effect on the active absorption or secretion of glucose or electrolytes. Pharmacology The primary mode of action is thought to be through the osmotic effect of polyethylene glycol 3350 which causes water to be retained in the colon and produces a watery stool. Polyethylene Glycol induces as diarrhea which rapidly cleanses the bowel, usually within four hours. Dosage The usual dose of Polyethylene Glycol is 17 gm of powder per day (or as directed by physician) in a glass of water, juice, coke, coffee or tea. Each bottle of Polyethylene Glycol is supplied with a cup that is used to measure 17 gm or 8.5 gm of laxative powder when filled upto the marked line. Administration It should always be taken by mouth. Measure the dose using the supplied cup, stir and dissolve in a glass of water, juice, coke, coffee or tea. Taking more than the prescribed dose may cause loss of fluid due to severe diarrhea. Interaction No specific drug interactions have been demonstrated. Contraindications Polyethylene glycol is contraindicated in patients with known or suspected bowel obstruction and patients known to be allergic to polyethylene glycol. Side Effects Nausea, abdominal bloating, cramping and flatulence may occur. High doses may produce diarrhea and excessive stool frequency, particularly in elderly nursing home patients. Patients taking other medications containing polyethylene glycol have occasionally developed urticaria suggestive of an allergic reaction. Pregnancy & Lactation Pregnancy: It is not known whether Polyethylene glycol can cause fetal harm when administered to a pregnant woman, or can effect reproductive capacity. Polyethylene glycol should only be administered to a pregnant woman if clearly needed.Lactation: There is no information on the use of Polyethylene glycol while nursing. Consultation with a physician is necessary in case of breastfeeding. Precautions Patients with symptoms suggestive of bowel obstruction (nausea, vomiting, abdominal pain or distention) should be evaluated to rule out this condition before initiating Polyethylene Glycol therapy. Polyethylene Glycol should be administered after being dissolved in water, juice, coke, coffee or tea. Overdose Effects There have been no reports of accidental overdosage. In the event of overdosage diarrhea would be the expected major event. If an overdose of drug occurred without concomitant ingestion of fluid, dehydration due to diarrhea may result. Medication should be terminated and free water administered. Duration of Treatment Polyethylene Glycol achieves its best results when used between one and two weeks. It may be discontinued after several satisfactory bowel movements. Should unusual cramps, bloating, or diarrhea occur, consultation with physician is needed. Polyethylene Glycol is intended for up to a two-week course of therapy. It should not be used for a longer time unless directed by a physician. After successfully completing the Polyethylene Glycol therapy (usually between one and two weeks) discussion with a physician is needed to change lifestyle ..

Tk.120.00/=

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Aripra 10 Tablet

Aripra 10 Tablet

Indications Aripiprazole is indicated for- SchizophreniaSchizoaffective disorderAcute manic and mixed episodes associated with Bipolar I DisorderMaintaining efficacy in patients with Bipolar I Disorder who are stabilized Therapeutic Class Atypical neuroleptic drugs Pharmacology Aripiprazole is an atypical antipsychotic that has both dopamine and serotonin receptors activity. It is a partial agonist of dopamine D2 receptors that relieves the symptoms of schizophrenia. It is characterized as a dopamine system stabilizer. It is a potent partial agonist at serotonin 5-HT1A receptors and antagonist at 5-HT2A receptors. This is associated with improvement of depressive, cognitive and negative symptoms. Dosage & Administration For Schizophrenia: 10 to 15 mg, once daily, without regard to food. Dose increment should not be made before 2 weeks, the time needed to achieve steady state.For Bipolar mania: 30 mg, once daily, without regard to food. Interaction Caution should be exercised when aripipazole is taken in combination with other centrally acting drugs and alcohol. Carbamazepine could cause an increase in aripiprazole clearance and lower blood levels. Ketoconazole, quinidine, fluoxetine or paroxetine can inhibit aripiprazole elimination and cause increased blood levels. Contraindications Aripiprazole is contraindicated in patients who are hypersensitive to it or to any component of this product. Side Effects Headache, constipation, asthenia, nausea, dyspepsia, vomiting, coughing, abdominal pain. Pregnancy & Lactation Aripiprazole should not be used in pregnancy as no human trial is performed. Patients should be advised not to breast feed an infant if they are taking aripiprazole. Precautions Aripiprazole may be associated with orthostatic hypotension (orthostatic lightheadedness).Aripiprazole should be used with caution in patients with known cardiovascular disease (myocardial infarction or ischaemic heart disease, heart failure or conduction abnormalities), cerebrovascular disease, or conditions that would predispose patients to hypotension (dehydration, hypovolemia, and treatment with antihypertensive medications).Seizures occurred in aripiprazole-treated patients. As with other antipsychotic drugs, aripiprazole should be used cautiously in patients with Alzheimer's dementia.Aripiprazole is not approved for the treatment of patients with dementia-related psychosis. Overdose Effects Aripiprazole at doses up to 1080 mg causes no fatalities. The signs and symptoms observed with aripiprazole overdose included nausea, vomiting, asthenia, diarrhea, and somnolence. ..

Tk.5.00/=

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Aripra 15 Tab

Aripra 15 Tab

Aripra 15 Tab..

Tk.7.00/=

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Aritone Z  tablet

Aritone Z tablet

Aritone Z..

Tk.3.00/=

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Arofil 200 SR Tab

Arofil 200 SR Tab

Arofil 200 SR Tab..

Tk.1.60/=

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Arofil SR 300 Tab

Arofil SR 300 Tab

Arofil SR 300 Tab..

Tk.2.35/=

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Arofil SR 400 Tab

Arofil SR 400 Tab

Arofil SR 400 Tab..

Tk.2.98/=

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Arpolax Tablet

Arpolax Tablet

Arpolax..

Tk.8.00/=

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Artemet

Artemet

Artemet..

Tk.20.00/=

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Askorel 100 ml Syp

Askorel 100 ml Syp

Askorel 100 ml Syp..

Tk.80.00/=

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Askorel SR Tab

Askorel SR Tab

Askorel SR Tab..

Tk.10.00/=

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Azecol Cap

Azecol Cap

Azecol Cap..

Tk.10.00/=

  0 отзывов

AztaCap

AztaCap

AztaCap..

Tk.22.00/=

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Barbit 30 tab

Barbit 30 tab

Barbit 30 tab..

Tk.0.78/=

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Barbit 60 Tab

Barbit 60 Tab

Barbit 60 Tab..

Tk.1.14/=

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Barbit Elixir 100ml

Barbit Elixir 100ml

Barbit Elixir 100ml..

Tk.57.00/=

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Barbit Elixir 50ml

Barbit Elixir 50ml

Barbit Elixir 50ml..

Tk.29.06/=

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Barbit IV/IM inj

Barbit IV/IM inj

Barbit IV/IM inj..

Tk.80.00/=

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Benadip 10/5 cap.

Benadip 10/5 cap.

Benadip 10/5 cap...

Tk.6.00/=

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Besiven Eye Drop

Besiven Eye Drop

Besiven Eye Drop..

Tk.350.00/=

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Betaderm N Oint.

Betaderm N Oint.

Betaderm N Oint...

Tk.22.00/=

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Betaderm Oint.

Betaderm Oint.

Betaderm Oint...

Tk.35.00/=

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Betamesal Scalp Lotion

Betamesal Scalp Lotion

Betamesal Scalp Lotion..

Tk.150.00/=

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Betastin Eye Drop

Betastin Eye Drop

Betastin Eye Drop..

Tk.300.00/=

  0 отзывов

Beuflox 250

Beuflox 250

Beuflox 250..

Tk.8.50/=

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