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A COF Syrup100 ml.
A COF 100 ml.CompositionEach 5 ml contains Dextromethorphan Hydrobromide BP 20 mg, Phenylephrine Hydrochloride BP 10 mg and Triprolidine Hydrochloride BP 2.5 mg.PHARMACOLOGYDextromethorphan Hydrobromide is a cough suppressant used to treat coughing. Phenylephrine Hydrochloride stimulates postsynaptic alpha-receptors, resulting in vasoconstriction, which reduces nasal congestion. Triprolidine Hydrochloride is a sedating antihistamine which is used for the symptomatic relief from allergic rhinitis.IndicationsTemporarily relieves these symptoms due to common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:• cough due to minor throat of bronchial irritation• runny nose• sneezing• itching of the nose or throat• itchy, watery eyes• nasal congestion• reduces swelling of nasal passagesDose and AdministrationRoute of Administration : Oral. Adults & Children 12 years of age and older : 1 teaspoonful (5 ml) every 4 hours. Children 6 to under 12 years age : ½ teaspoonful (2.5 ml) every 4 hours. Or as directed by the physician. Contraindications• Patients with hypersensitivity to Dextromethorphan Hydrobromide, PhenylephrineHydrochloride and Triprolidine Hydrochloride.• Persons under treatment with Monoamine Oxidase Inhibitor (MAO) within 2 weeks of stopping such treatment.Precaution and WarningAs with other sympathomimetic agents, caution should be exercised in patients with hypertension, heart disease, diabetes, thyroid disease or glaucoma. This combination should not be used for persistent or chronic cough which occurs with smoking, asthma, chronic bronchitis or for a couth with excessive secretion of phlegm unless directed by a physician. Precaution should be taken for persons with trouble urinating due to an enlarged prostate gland. This combination may impair the patients ability to drive and also to operate machinery.Side EffectsCommon Side Effects : It may cause drowsiness, dottiness and constipation. Other side effects that may occur include GIT discomfort. Rare Side Effects : Other less common side effects may include transient hypertension, dry mouth, restlessness, palpitations, allergic reactions such as rashes, tightness of chest, thickening of bronchial secretions, toxic psychosis and blood dyscrasia. Use in Pregnancy & Lactation There are no specific data on use of this combination during pregnancy and lactation. Use in children & adolescents Not to be used in children below 2 years old. To be used with caution, and as advised by the physician for children age 2 to 6 years.Drug InteractionWith medicine : Taking certain MAO inhibitors with this medication may cause a serious (possibly fatal) drug interaction. Avoid taking isocarboxazid, methylene blue, moclobemide, phenelzine, procarbazine, rasagiline, selegiline, or tranylcypromine during treatment with this medication. Most MAO inhibitors should also not be taken for two weeks before treatment with this medication. Caution should be excercised while taking this drug with antihistamines applied to the skin (such as diphenhydramine cream, ointment, spray), antispasmodics (e.g. atropine, belladonna alkaloids), beta blockers (e.g. metoprolol, atenolol), drugs for Parkinson’s disease (e.g. anticholinergics such as benztropine, trihexyphenidyl), guanethidine, certain inhaled anesthetics (e.g. halothane), methyldopa, reserpine, scopolamine, tricyclic antidepressants (e.g. amitriptyline, desipramine), anti-seizure drugs (e.g. carbamazepine), medicine for sleep or anxiety (e.g. alprazolam, diazepam, zolpidem), muscle relaxants, narcotic pain relievers (e.g. codeine), psychiatric medicines (e.g. chlorpromazine, risperidone, amitriptyline, trazodone). With food and others : There is no data found on interaction with food of this medicine.Over dosageIn cases of over dosage, hospital admission is strongly advised. Over dosage may produce respiratory depression, paranoid psychosis, delusions, hallucinations, and convulsion. Treatment should include emptying the stomach by aspiration or gastric lavage. Nervous stimulation and convulsions should be treated with a sedative such as diazepam intramuscularly. If marked excitation is present, a sedative such as diazepam or a short-acting barbiturate may be given. Severe over dosage of phenylephrine hydrochloride may produce hypertension and associated reflex bradycardia. Treatment measures include early gastric lavage and symptomatic and supportive measures. The hypertensive effects may be treated with an alpha receptor blocking agent (such as phentolamine mesilate 6-10 mg) given intravenously, and the bradycardia treated with atropine, preferable only after the pressure has been controlled.StorageKeep all medicines out of reach of children. Store below 300 C., Protect from light.PackingEach bottle contains 100 ml syrup. ..
Tk.100.00/=
A Phenicol 10 ml Eye Drops
A PhenicolDESCRIPTIONChloramphenicol is a broad spectrum antibiotic, isolated in 1947 from streptomyces venezuelae. It is primarily bacteriostatic and acts by inhibition of protein synthesis. It has been noted that chloramphenicol is found in measurable amounts in the aqueous humor following local application to the eye. Development of resistance to Chloramphenicol is minimum for staphylococci and many other species of bacteria.COMPOSITIONEYE OINTMENT : Each gm contains 10 mg of Chloramphenicol BP in a special base. It is a sterile eye ointment.EYE/EAR DROPS : Each ml eye/ear drops contains Chloramphenicol BP 5 mg. It is a sterile eye / ear drops.INDICATIONSA-PHENICOL is indicated in surface ocular infections involving the conjunctiva and/or cornea caused by Chloramphenicol susceptible organisms. A-PHENICOL is also active against common bacterial pathogens, E.coli, Klebsiella, Niesseria sp., H.influenzae, Enterobacter sp., Staphylococcus aureus and Streptococcus pneumoniae.A-PHENICOL is also indicated in ear canal infection.DOSAGE AND ADMINISTRATIONA-PHENICOL Eye OintmentA PHENICOL eye ointment should be used every three hours. Administration should be continued day and night for the first 48 hours after which the interval between application may be increased and continued for at least 2 days after the eye appears normal.A-PHENICOL Eye/Ear DropsFor eye : 2 drops of solution every 1 hour, until condition improves or instill 4 times daily depending on severity of infection. For ear : (Adult & Children) : 2 or 3 drops in the affected ear 2-3 times daily. OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONSChloramphenicol is contraindicated in patients sensitive to any of its components.PRECAUTIONSOphthalmic ointments may retard corneal wound healing. So patients with corneal disease should take precautions while using this medicine.SUPPLYA-PHENICOL Eye Ointment : A-PHENICOL Eye Ointment is supplied in 5 gmcollapsible tube.A-PHENICOL Eye/Ear Drops : A-PHENICOL Eye/Ear Drops is supplied in 10 mlplastic bottle with dropper...
Tk.34.50/=
A Spasm 5 mg Tablet
A Spasm 5 mg TabletIndicationsAbdominal pain, Colic, Gastrointestinal tract spasm, Peptic ulcer disease, Visceral spasmsPharmacologyOxyphenonium is an anticholinergic drug, a medication that reduces the effect of acetylcholine, a chemical released from nerves that stimulates muscles, by blocking the receptors for acetylcholine on smooth muscle (a type of muscle). It also has a direct relaxing effect on smooth muscle. Oxyphenonium is used to treat or prevent spasm in the muscles of the gastrointestinal tract in the irritable bowel syndrome. In addition, Oxyphenonium inhibits gastrointestinal propulsive motility and decreases gastric acid secretion and controls excessive pharyngeal, tracheal and bronchial secretions.ContraindicationsUrinary outflow obstruction, paralytic ileus, myasthenia gravis.Side EffectsDryness of mouth, difficulty in talking/swallowing; reduced bronchial secretions; blurring of vision, photophobia; bradycardia followed by tachycardia and arrhythmias; urinary retention, constipation, vomiting, nausea; confusion and giddiness...
Tk.1.50/=
A Tetra 1% 5 gm Ointment
A Tetra 1%DESCRIPTIONA-TETRA (Tetracycline) is a semi-synthetic Tetracycline produced from Chlortetracycline. It is an antibiotic isolated from Streptomyces aureo-faciens. It is a broad spectrum antibiotic which is active against a wide range of Gram-negative and Gram-positive bacteria. Tetracycline has its main mechanism of action on protein synthesis, and an energy-dependent active transport system pumps the drug through the inner cytoplasmic membrane of the bacteria. Once inside the bacterial cell, Tetracycline inhibits protein synthesis by binding specifically to 30S ribosome. The drug appears to prevent access of aminoacyl tRNA to the acceptor site on the mRNA-ribosome complex. This prevents the addition of amino acid to the growing peptide chain.COMPOSITIONCapsule : Each capsule contains Tetracycline Hydrochloride BP 500 mg.Tablet : Each tablet contains Tetracycline Hydrochloride BP 500 mg.INDICATIONSA-TETRA is a bacteriostatic antibiotic with a broad spectrum of activity against bacteria, and also has some anti-protozoal activities. It remains the choice in the treatment of Chlamydia, Rickettsia, Mycoplasma, Brucella and some Spirochaetal infections. A number of Gram-negative and Grampositive pathogens can be treated with Tetracycline. It has been given long term in the management of severe acne.When Penicillin is contraindicated, the Tetracyclines are alternative drugs in the treatment of infection.DOSAGE AND ADMINISTRATIONCapsule : The usual dose is 1 to 2 g/day (2-4 capsules) divided in 2 or 4 equal doses depending on the severity of the infection, preferably one hour before or two hours after meals with a glass of water.Tablet : 1-1/2 tablet (250-500 mg) should be taken after 6 hours. Preferably one hour before or two hours after meal with a glass of water.OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSCommon side effects are gastro-intestinal disturbances including nausea, vomiting and diarrhoea. These are common especially with high doses and most are attributed to irritation of the mucosa. Other effects that have been reported are dry mouth, glossitis and discoloration of the tongue,stomatitis and dyspepsia. Benign intracranial hypertension, pancreatitis and pseudomembranous colitis are reported.CONTRAINDICATIONSTetracycline is contraindicated in patients hypersensitive to any of its group. It should be avoided in patients with systemic lupus erythematosus. It is also contraindicated in severe renal impairment, if given, doses should be reduced.PRECAUTIONSCare should be taken if Tetracycline is given to patients with impaired liver function.Potential hepatotoxic drugs including Erythromycin, Chloram-phenicol, Isoniazid, Sulfonamide etc. should not be given concomitantly. The risk of nephrotoxicity may be increased if given with Methoxyflurane or other potentially nephrotoxic medication. Care is advisable in patients with Myasthenia gravis, who may be at risk of neuromuscular blockade.WARNINGSThe use of Tetracycline hydrochloride during tooth development (last half of pregnancy, infancy and childhood to the age of 8 years) may cause permanent discoloration of the teeth.DRUG INTERACTIONSIt has been reported that Tetracycline in combination with Methoxyflurane have resulted in nephrotoxicity. Milk and milk products as well as antacids containing calcium, aluminium and magnesium impair the absorption of Tetracycline and resulting decreased serum levels. Tetracycline inhibits the antimicrobial activity of penicillin when used concomitantly...
Tk.12.00/=
A-B1 100 mg Tablet, 1 strip
A-B1 100 mg Tablet, 1 stripDESCRIPTIONA-B1 (Thiamine Hydrochloride) is a water soluble vitamin. It is an organicmolecule which contains a pyrimidine and a thiazole nucleus linked by amethylene bridge. It occurs as small white hygroscopic crystals orcrystalline powder that usually has a slight characteristic odour. Itfunctions in the body in the form of coenzyme Thiamine pyrophosphate.Thiamine pyrophos-phate serves as a coenzyme in carbohydratemetabolism by decar-boxylation of a-keto acids such as pyruvate anda-ketoglutarate which leads to the formation of acetyl CoA. Thiamine orVitamin B1 also participates in the formation or degradation of a-ketols bytransketolase. Vitamin B1 is essential for metabolism of carbohydrate.Recommended daily intake of Thiamine is 0.5mg/1000 kcal. Majorsymptoms of Thiamine deficiency are related to the nervous system (Dryberiberi) and to the cardiovascular system (Wet beriberi).COMPOSITIONEach tablet contains Thiamine Hydrochloride BP 100 mg.INDICATIONSInfantile beriberi : Loss of appetite, vomiting, greenish stools, followed byparoxysmal attacks of muscular rigidity.Adult beriberi : Dry skin, discomfort, confabulation followed by paralysis.Wernicke's encephalopathy : Neuropsychiatric disorder may develop insome cases due to alcohol intake.Korsakoff's syndrome : Diabetes, cancer and in other cases for examplethe patients having nutritional intake parenterally where Vitamin B1 isabsent may arise Vitamin B1 deficiency.Fatigue, anorexiaGastrointestinal disturbanceNeurological disorderOther Vitamin B1 deficiency in case of pregnancy and lactation.DOSAGE AND ADMINISTRATIONMild to moderate chronic deficiency : ¼ tablet daily.Severe deficiency : 2-3 tablets daily.OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSNo known side effect have yet been established.CONTRAINDICATIONSA-B1 is contraindicated in patients who are hypersensitive to it.SUPPLYEach box contains 10 x 10 tablets in blister strip...
Tk.8.60/=
A-Cal 500 mg Tab
A-Cal 500 mg TabDESCRIPTIONCalcium is an essential body electrolyte. It is involved in the maintenance of normal muscle and nerve function, cardiac function and is essential to blood coagulation.Calcium Carbonate has three main actions: it supplements dietary calcium, neutralizes gastric acid in peptic ulcer disease and sequesters phosphorous in the intestine to reduce total body phosphate accumulation in chronic renal failure. Calcium requirement varies with age and is relatively greater in childhood, pregnancy and lactation dueto an increased demand, in old age due to impaired absorption, and as phosphate binder in patients with renal failure. Absorption depends on previous intake of calcium, other nutrients, pregnancy, lactation, overall calcium balance and availability of vitamin D.COMPOSITIONA-CAL 250 chewable : Each chewable tablet contains Calcium Carbonate BP 0.625 g equivalent to 250 mg elemental Calcium. A-CAL 250 : Each film-coated tablet contains Calcium Carbonate BP 0.625 g equivalent to 250 mg elemental Calcium. A-CAL 500 : Each film-coated tablet contains Calcium Carbonate BP 1.25 g equivalent to 500 mg elemental Calcium.INDICATIONSIn calcium deficiency states : Treatment of calcium deficiency states including osteomalacia, rickets and mal-absorption syndromes affecting the upper gastrointestinal tract.As therapeutic supplementation : During times when intake may be inadequate, particularly those associated with the increased demand of childhood, old age, pregnancy and lactation. As a phosphate binder : As effective phosphate binder given by mouth to reduce phosphate absorption from the gut in patient with hyperphosphataemia, chronic renal failure in order to prevent the development of renal osteo-dystrophy. Osteoporosis : An adjunct to conventional therapy in the arrest or slowing down of bone demineralisation in osteoporosis or when other effective treatment is contraindicated. As an antacid : Usually in association with other antacids, especially magnesium containing antacids.DOSAGE AND ADMINISTRATIONA-Cal 250 :Adults : 2 tablets daily.Children : 1-2 tablets daily.A-Cal 500 : 1 tablet daily.OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSMild gastrointestinal disturbances may occur rarely (e.g. nausea, abdominal pain, constipation, flatulence and eructation etc.)CONTRAINDICATIONSCalcium Carbonate is contraindicated in hypercalcemia and hyperparathyroidism, hypercalcemia and nephrolithiasis, Zollinger Ellison Syndrome etc.PRECAUTIONSShould be used with caution in patients with impaired renal function, a history of stone formation should also be recommended to increase their fluid intake. High doses of vitamin D should be avoided during calcium therapy unless specially indicated. In case of hypercalciuria the dosage should be reduced or treatment stopped.USE IN PREGNANCY AND LACTATIONCalcium supplements have been in wide use for many years without apparent ill consequence.DRUG INTERACTIONSCalcium Carbonate and other antacids may interfere with the absorption of concomitantly administered tetracycline preparations or ciprofloxacin. This can be minimized by giving Calcium Carbonate and the other medication 2 to 3 hours apart.SUPPLYA-CAL 250 chewable : Each box contains 3 X 10 tablets in blisterstrips.A-CAL 250 : Each box contains 10 X 10 tablets in blister strips.A-CAL 500 : Each box contains 10 X 10 tablets in blister strips...
Tk.5.00/=
A-Cal 500/400 IU Tablet DX 30's pack
A-Cal 500/400 IU Tablet DX 30's packDESCRIPTIONA-Cal DX tablet is a special preparation of Calcium and Vitamin D3. Calcium is an essential nutrient that helps to build and maintain healthy teeth and bones. It makes body’s framework stronger by building bone.COMPOSITIONEach film-coated tablet contains Calcium Carbonate BP equivalent to elemental Calcium 500 mg and Vitamin D3 (Cholecalciferol) BP 400 IU.INDICATIONFor the prevention and/or treatment of osteoporosis,fractures,osteomalacia,rickets,tetany,pse udo-parathyroidism, for healthy bone formation and maintenance and other calcium and/or vitamin D deficiencies and to meet increased needs of calcium and/or vitamin D. Dosage and Administration: The recommended starting dose of A-Cal DX (Calcium 500 mg & Vitamin D 400 IU) 1 tablet twice daily, preferably with or just after meals.SIDE EFFECTSThe use of calcium supplements may cause constipation, and headache; mild hypercalcemia associated with anorexia, nausea and vomiting; more severe hypercalcemia associated with confusion, delirium, stupor and coma. The use of vitamin D may cause weakness, headache, somnolence, nausea, vomiting, dry mouth, constipation, muscle pain, bone pain, metallic taste, polyuria, polydipsia, anorexia, weight loss, nocturia and mild acidosis. CONTRAINDICATION A-Cal DX is contraindicated in patients Having hyperalcaemia, severe hypercalciurea, ventricular fibrillation, hypervitaminosis, severe renal failure and kidney stones and hypersensitivity to any of the ingredients of the product.PRECAUTIONPatients with mild to moderate renal failure or mild hypercalciuria should be supervised carefully. Periodic checks of plasma calcium levels and urinary calcium excretion should be made in patient with a history of renal stones or in patients with mild to moderate renal failure or mild hypercalciuria. USE IN PREGNANCY AND LACTATION A-Cal DX should be used under the direction of a physician during pregnancy and lactation. During pregnancy, doses of vitamin D greater than the recommended dietary allowance should be used only when clearly needed.DRUG INTERACTIONCo-administration of calcium with some drugs such as tetracycline antibiotics (e.g., doxycycline, minocycline), estramustine, levothyroxine, and quinolone antibiotics (e.g. ciprofloxacin, levofloxacin) can decrease the absorption of both calcium and the co-administered drug. Certain medications can decrease the absorption of vitamin D e.g., bile acid sequestrates such as cholestyramine/colestipol, ketoconazole, mineral oil, orlistat. Certain drugs can accelerate the absorption of vitamin D e.g. phenytonin, phenobarbital.SUPPLYEach plastic container contains 30 tablets...
Tk.225.00/=
A-Cal D 30s Tab
A-Cal D 30s TabDESCRIPTIONA-CAL D tablet is a special preparation of Calcium and Vitamin D3. Calcium is an essential nutrient that helps to build and maintain healthy teeth and bones. It makes body's framework stronger by building bone. Most notably, Calcium helps to reduce the risk of osteoporosis, a disease that's characterized by a decrease in bone mass and an increase in bone fractures. Calcium also plays a role in muscle contraction, blood clotting and nerve function.Vitamin D3 is essential for healthy bones as it aids in calcium absorption from the GI tract. In addition to this it stimulates bone formation. Controlled clinical studies showed that Calcium and Vitamin D3 has synergistic effects on bone growth as well as in osteoporosis and fracture prevention.COMPOSITIONEach film-coated tablet contains elemental Calcium 500 mg and Vitamin D3 200 IU.INDICATIONSPrevention and treatment of osteoporosis and fractures (both vertebral and non-vertebral); treatment of osteomalacia, rickets, tetany, hypoparathyroidism and secondary hyperparathyroidism; in kidney disease, pancreatitis, hyperoxaluria; as phosphate binder to reduce phosphate absorption in patients with hyperphosphatemia; during therapy with antiseizure medications, bisphosphonates in paget's disease; for healthy bone formation and maintenance; in disorders of osteogenesis and tooth formation (in addition to specific treatment); inpregnancy and lactation due to increased demand; in raised calcium requirement for children and adolescents at times of rapid growth; to prevent and cure calcium deficiency and/or vitamin D deficiency especially in the household people who do not get direct sunlight. DOSAGE AND ADMINISTRATION Adults, Elderly and children: 1 tablet twice daily. OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSThe use of calcium supplements may cause constipation, and headache; mild hypercalcemia associated with anorexia, nausea and vomiting; more severe hypercalcemia associated with confusion, delirium, stupor and coma. The use of vitamin D may cause weakness, headache, somnolence, nausea, vomiting, dry mouth, constipation, muscle pain, bone pain, metallic taste, polyuria, polydipsia, anorexia, weight loss, nocturia and mild acidosis.PRECAUTIONSPatients with mild to moderate renal failure or mild hypercalciuria should be supervised carefully. Periodic checks of plasma calcium levels and urinary calcium excretion should be made in patients with a history of renal stones or in patients with mild to moderate renal failure or mild hypercalciuria. With long term treatment it is advisable to monitor serum and urinary calcium levels and kidney function and reduce or stop treatment temporarily if serum calcium level exceeds 12 mg/dl. Calcium salt should be used cautiously in patients with sarcoidosis, history of nephrolithiasis, cardiac disease and in patients receiving cardiac glycosides.CONTRAINDICATIONSIt is contraindicated in patients having hypercalcaemia and severe hypercalciurea, ventricular fibrillation, hypervitaminosis, severe renal failure, kidney stones and hypersensitivity to any of the ingredients of the product.DRUG INTERACTIONA-CAL D should not be used with the following medications because ofpossible interactions - Iron; digoxin; verapamil; calcium, aluminium or magnesium containing antacids; other calcium or vitamin D supplements (e.g., calcitriol). Bran decreases the gastrointestinal absorption of calcium and may therefore decrease the efficacy of calcium supplements. Concurrent administration of thiazide diuretics may increase the risk of hypercalcemia. Co-administration of calcium with some drugs such as tetracycline antibiotics (e.g., doxycycline, minocycline), estramustine, levothyroxine, and quinolone antibiotics (e.g., ciprofloxacin, levofloxacin) can decrease the absorption of both calcium and the co-administered drug. Certain medications can decrease the absorption of vitamin D e.g., bile acid sequestrates such as cholestyramine/ colestipol, ketoconazole, mineral oil, orlistat. Certain drugs can accelerate the absorption of vitamin D e.g., phenytoin, phenobarbital.OVER DOSAGEIf calcium supplements are taken at overdose for long time then hypercalcimia and hypercalciuria may rise. Symptoms of overdosage of vitamin D supplements include weakness, lassitude, impaired memory, dementia, depression, paranoia, hallucinations, delirium and coma. In case of overdose supplement should be discontinued. Treatment includes saline administration, furosemide diuresis and sometimes corticosteroids.USE IN PREGNANCY AND LACTATIONA-CAL D should be used under the direction of a physician during pregnancy and lactation. Vitamin D and its metabolites pass into the breast milk in limited amounts.SUPPLY30 Tablet Pack : Each airtight plastic container contains 30 tablets.15 Tablet Pack : Each airtight plastic container contains 15 tablets...
Tk.195.00/=
A-CALM 50 mg Tablet
A-CALM 50 mg TabletDESCRIPTIONTolperisone hydrochloride is a centrally acting muscle relaxant, which acts on the central nervous system and used mainly for the treatment of elevated muscle tone and tension as well as for certain circulatory problems in the extremities. It reduces experimental hypertonia and decerebration and improves peripheral blood flow. The circulatory effect is supposed to be based on peripheral mechanism and is independent from the cerebral centers of vasoregulation.COMPOSITIONEach film-coated tablet contains Tolperisone hydrochloride INN 50 mg.INDICATIONSIncreased tone of skeletal muscles due to organic neurological disorders (e.g. injury of the pyramidal tract, multiple sclerosis, myelopathy, encephalomyelitis etc.), muscular hypertension, muscular spasm, muscular contraction & rigidity, spinal automatism and discopathy. Obliterate vascular diseases (obliterate arteriosclerosis, diabetic angiopathy, obliterative thromboangitis, raynaud's disease, diffusion scleroderma) and disorders due to injury innervation of the vessels (acrocyanosis, intermittent angioneurotic dysbasia). In individual cases post thrombotic venous and circulation disorders and crural ulcer.DOSAGE AND ADMINISTRATIONOne should follow the doctor's instructions regarding the dosage of Tolperisone hydrochloride. The recommended dose is as followings: Adult: 50-150 mg three times daily according to the individual requirement and tolerance of the patients. Children: (from 6 to 14 years): 2-4 mg/kg/day in three divided doses. Children: (from 3 months to 6 years): 5-10 mg/kg/day in three divided doses.SIDE EFFECTSSometimes muscular weakness, headache, nausea, vomiting, and rarely hypersensitivity reactions.CONTRAINDICATIONSHypersensitivity to Tolperisone, Myasthenia gravis, nursing mother. PRECAUTIONS Incase of children, the prescribed dose and duration of treatment should closely be observed.USE IN PREGNANCY AND LACTATIONTolperisone hydrochloride should be used in pregnancy to physician's advice. Tolperisone hydrochloride should not be used during breastfeeding.DRUG INTERACTIONConcomitant use of methocarbamol with tolperisone hydrochloride has been reported to cause disturbance of visual accommodation.SUPPLYEach box contains 5 x 10 tablets in blister strips..
Tk.6.00/=
A-clox 500 mg cap
A-clox 500 mg capDESCRIPTIONA-CLOX is a bactericidal antibiotic that is particularly useful against penicillinase producing Staphylococci. It is a semisynthetic member of the penicillin family. It kills bacteria by interfering the synthesis of the bacterial cell wall. A-CLOX is widely used against Gram-positive bacteria.COMPOSITIONA-CLOX capsule : Each capsule contains Cloxacillin Sodium BP equivalent to Cloxacillin 500 mg.A-CLOX Powder for Syrup : Each 5 ml contains Cloxacillin Sodium BP equivalent to 125 mg Cloxacillin after reconstitution.A-CLOX 250 mg Injection : Each vial contains sterile Cloxacillin Sodium BP equivalent to 250 mg Cloxacillin.A-CLOX 500 mg Injection : Each vial contains sterile Cloxacillin Sodium BP equivalent to 500 mg Cloxacillin.INDICATIONS Respiratory tract infection : Bronchitis Bronchiectasis, otitis media, sinusitis, pneumonia, tonsillitis, pharyngitis. Skin and soft tissue infections : Cellulitis, styes, furuncles, pemphigus, breast abscess, carbuncles, infected burns. Other infections : Osteomyelitis, acute and subacute endocarditis, urinary tract infections, obstetric infections, prophylaxis in neonatal infections.DOSAGE AND ADMINISTRATIONAdults : Oral : 500 mg six hourly ½ -1 hour before meals Intramuscular injection : 250 mg every 4-6 hours. Intravenous injection : 500 mg every 4-6 hours. In serious infections dosage may be doubled. Children (2-10 years) : 1-2 tea spoonful 6 hourly or ½ of the adult dose. Upto 2 years : ¼ of the adult dose.OR AS DIRECTED BY THE PHYSICIANInjection AdministrationFor Intramuscular injection : 250 mg and 500 mg are to be dissolved with 1.5 ml and 2 ml water for injection BP respectively before administration. For Intravenous injection : 500 mg is to be dissolved with 5-8 ml water for injection BP administered by slow injection for 3 to 4 minutes. Adequately diluted A-CLOX injection can be administered into the drip tube slowly over a period of 3 to 4 minutes.CONTRAINDICATIONSCloxacillin is contraindicated to Penicillin hypersensitive patients.SIDE EFFECTOccasional rashes, nausea, diarrhoea or indigestion may rarely be reported.SUPPLYCapsule : Box containing 1010 capsules in stripsPowder for Syrup : Bottle containing required amount of powder toprepare 100 ml syrup.A-CLOX 250 mg injection : Box contains 5 blister packs each containingone vial and one 5 ml ampoule of water for injection.A-CLOX 500 mg injection : Box contains 5 blister packs each containingone vial and one 5 ml ampoule of water for injection...
Tk.5.98/=
A-Cof 100ml Syp
A-Cof 100ml SypCompositionEach 5 ml contains Dextromethorphan Hydrobromide BP 20 mg, Phenylephrine Hydrochloride BP 10 mg and Triprolidine Hydrochloride BP 2.5 mg.PHARMACOLOGYDextromethorphan Hydrobromide is a cough suppressant used to treat coughing. Phenylephrine Hydrochloride stimulates postsynaptic alpha-receptors, resulting in vasoconstriction, which reduces nasal congestion. Triprolidine Hydrochloride is a sedating antihistamine which is used for the symptomatic relief from allergic rhinitis.IndicationsTemporarily relieves these symptoms due to common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:• cough due to minor throat of bronchial irritation• runny nose• sneezing• itching of the nose or throat• itchy, watery eyes• nasal congestion• reduces swelling of nasal passagesDose and Administration Route of Administration : Oral. Adults & Children 12 years of age and older : 1 teaspoonful (5 ml) every 4 hours. Children 6 to under 12 years age : ½ teaspoonful (2.5 ml) every 4 hours. Or as directed by the physician. Contraindications• Patients with hypersensitivity to Dextromethorphan Hydrobromide, PhenylephrineHydrochloride and Triprolidine Hydrochloride.• Persons under treatment with Monoamine Oxidase Inhibitor (MAO) within 2 weeks of stopping such treatment.Precaution and WarningAs with other sympathomimetic agents, caution should be exercised in patients with hypertension, heart disease, diabetes, thyroid disease or glaucoma. This combination should not be used for persistent or chronic cough which occurs with smoking, asthma, chronic bronchitis or for a couth with excessive secretion of phlegm unless directed by a physician. Precaution should be taken for persons with trouble urinating due to an enlarged prostate gland. This combination may impair the patients ability to drive and also to operate machinery.Side EffectsCommon Side Effects : It may cause drowsiness, dottiness and constipation. Other side effects that may occur include GIT discomfort. Rare Side Effects : Other less common side effects may include transient hypertension, dry mouth, restlessness, palpitations, allergic reactions such as rashes, tightness of chest, thickening of bronchial secretions, toxic psychosis and blood dyscrasia. Use in Pregnancy & Lactation There are no specific data on use of this combination during pregnancy and lactation. Use in children & adolescents Not to be used in children below 2 years old. To be used with caution, and as advised by the physician for children age 2 to 6 years.Drug InteractionWith medicine : Taking certain MAO inhibitors with this medication may cause a serious (possibly fatal) drug interaction. Avoid taking isocarboxazid, methylene blue, moclobemide, phenelzine, procarbazine, rasagiline, selegiline, or tranylcypromine during treatment with this medication. Most MAO inhibitors should also not be taken for two weeks before treatment with this medication. Caution should be excercised while taking this drug with antihistamines applied to the skin (such as diphenhydramine cream, ointment, spray), antispasmodics (e.g. atropine, belladonna alkaloids), beta blockers (e.g. metoprolol, atenolol), drugs for Parkinson’s disease (e.g. anticholinergics such as benztropine, trihexyphenidyl), guanethidine, certain inhaled anesthetics (e.g. halothane), methyldopa, reserpine, scopolamine, tricyclic antidepressants (e.g. amitriptyline, desipramine), anti-seizure drugs (e.g. carbamazepine), medicine for sleep or anxiety (e.g. alprazolam, diazepam, zolpidem), muscle relaxants, narcotic pain relievers (e.g. codeine), psychiatric medicines (e.g. chlorpromazine, risperidone, amitriptyline, trazodone). With food and others : There is no data found on interaction with food of this medicine.Over dosageIn cases of over dosage, hospital admission is strongly advised. Over dosage may produce respiratory depression, paranoid psychosis, delusions, hallucinations, and convulsion. Treatment should include emptying the stomach by aspiration or gastric lavage. Nervous stimulation and convulsions should be treated with a sedative such as diazepam intramuscularly. If marked excitation is present, a sedative such as diazepam or a short-acting barbiturate may be given. Severe over dosage of phenylephrine hydrochloride may produce hypertension and associated reflex bradycardia. Treatment measures include early gastric lavage and symptomatic and supportive measures. The hypertensive effects may be treated with an alpha receptor blocking agent (such as phentolamine mesilate 6-10 mg) given intravenously, and the bradycardia treated with atropine, preferable only after the pressure has been controlled.StorageKeep all medicines out of reach of children. Store below 300 C., Protect from light.PackingEach bottle contains 100 ml syrup. ..
Tk.100.00/=
A-Cold 100ml Syp
A-Cold 100ml SypDESCRIPTIONA-Cold (Bromhexine Hydrochloride) is a highly effective mucolytic expectorant syrup. It reduces the viscosity of sputum. It is rapidly absorbed from the gastrointestinal tract. It crosses the blood brain barrier and small amounts cross the placenta.COMPOSITIONEach 5 ml syrup contains Bromhexine Hydrochloride BP 4 mg.INDICATIONSA-Cold (Bromhexine Hydrochloride) syrup is a mucolytic used in the treatment of respiratory disorders associated with productive cough. It is also indicated in the chronic bronchitis, acute & chronic bronchopulmonary diseases, pneumoconiosis and pulmonary emphysema.DOSAGE & ADMINISTRATIONAdults The recommended dose is 2 to 4 teaspoonful 3 times daily. Initially 4 teaspoonful 3 times daily and then as required. Children 5-10 years : 1 teaspoonful 3 times daily. 2-5 years : 1/2 teaspoonful 3 times daily. Under 2 years : 1/4 teaspoonful 3 times daily.OR AS DIRECTED BY THE PHYSICIAN. SIDE-EFFECTSGastro-intestinal side effects may occur occasionally with Bromhexine and a transient rise in serum aminotransferase values has been reported. Other reported adverse effects include headache, dizziness, sweating, and skin rashes.CONTRAINDICATIONSBromhexine Hydrochloride is contra-indicated in-patients with known hypersensitivity to any of the components of the drug.PRECAUTIONSSince mucolytics may disrupt the gastric mucosal barrier, Bromhexine should be used with care in-patients with a history of peptic ulceration. Care is also advisable in asthmatic patients. Clearance of Bromhexine or its metabolites may be reduced in patients with severe hepatic or renal impairment.SUPPLYEach pet bottle contains 100 ml syrup..
Tk.40.12/=
A-Fenac 25 mg Tab
A-Fenac 25DESCRIPTIONA-FENAC (Diclofenac Sodium) is a potent nonsteroidal, anti-inflammatory agentwith analgesic and antipyretic properties. By virtue of its analgesic, antipyreticand anti-inflammatory properties together with its excellent tolerability marks amajor advance in the treatment of rheumatic and or inflammatory conditions.Diclofenac inhibits cyclooxygenase activity with a reduction in the tissueproduction of prostaglandins.Tablet A-FENAC is enteric-coated (acid-resistant coating) with the result that the active constituent is not released until it has passed through the stomach. A-FENAC SR tablet has got many advantages. Because the frequency of drug administration is reduced, patient compliance can be improved and drug administration be made more convenient as well.COMPOSITIONTablet : Each enteric coated A-FENAC 25 tablet contains Diclofenac Sodium BP 25 mg.Each enteric coated A-FENAC 50 tablet contains Diclofenac Sodium BP 50 mg.Tablet SR : Each A-FENAC SR (sustained release) tablet contains Diclofenac Sodium BP 100 mg.Injection : Each 3 ml ampoule of A-FENAC injection contains 75 mg Diclofenac Sodium BP.Suppository : A-Fenac 12.5 : Each suppository contains declofenac sodium BP 12.5 mg.A-Fenac 50 : Each suppository contains diclofenac sodium BP 50 mg.A-FENAC Gel : Each 100 g A-FENAC Gel contains Diclofenac Diethylamine BP1.16 g equivalent to Diclofenac Sodium 1 g.INDICATIONSA-FENAC is indicated in the following cases : Rheumatoid arthritis, osteoarthritis, low back pain, injuries and manifestations of soft tissue rheumatism, ankylosing spondylitis, acute gout, control of pain & inflammation in orthopaedic, dental & other minor surgery, juvenile rheumatoid arthritis, postoperative pain, renal colic & other musculoskeletal disorders.DOSAGE & ADMINISTRATIONUsual dosing information : Tablet A-FENAC should be taken with water during or immediately after meals. Antacid should not be taken within 1-2 hours aftertaking tablet A-FENAC.Usual adult dose :A-FENAC Tablet : In adults, the initial dose is 25-50 mg three times a day, depending on the severity of the condition.A-FENAC SR Tablet : 75-150 mg once daily.Injection : For adults the usual dose is 1 ampoule daily. In serious cases this dose may be increased up to 2 ampoules daily.Suppository :Adult : 75-150 mg daily in divided doses.Children (1-12 years) : 1-3 mg/kg daily in divided dosesGel :Adult (>12 years) : A small amount (2-4 g) of A-FENAC Gel should be applied 3- 4 times daily to the affected area and rubbed lightly. Treatment is dependent on the size of the affected area. A-FENAC Gel may also be given in addition to further treatment with other dosage forms of Diclofenac.OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONA-FENAC is contraindicated in peptic ulcer, previous sensitivity to Diclofenac Sodium and in asthmatic patients in whom attacks of asthma, urticaria or acute rhinitis are precipitated by Aspirin or other nonsteroidal anti-inflammatory agents with prostaglandin synthesis inhibiting activity.SIDE EFFECTSOccasional gastrointestinal disorders, headache, dizziness or vertigo, rash, elevation of SGOT/SGPT, rare peptic ulcer, gastro-intestinal bleeding, hepatitis, hypersensitivity reactions. In isolated cases, disturbances of sensation, erythema multiforme, purpura, abnormalities of renal function, blood dyscrasias may occur. PRECAUTIONSPrecaution should be taken in patients with symptoms/history of gastro-intestinal disease, impaired hepatic, cardiac or renal function, pregnancy, porphyria and patients who are taking diuretics, anticoagulant, or antidiabetics. During prolonged treatment, periodical monitoring of liver function should be carried out and blood counts are recommended. Possibility of hypersensitivity reactions to sodium disulphite particularly in patients with asthma.SUPPLYTablet :A-FENAC 25 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC 50 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC SR : Each box contains 10x10 tablets in blisters.Injection :A-FENAC : Each box contains 2x5 ampoules in blisters.Suppository :A-FENAC 12.5 : Each box contains 2x5 suppositories in blisters.A-FENAC 50 : Each box contains 2 x 5 suppositories in blisters.Gel :A-FENAC : Each tube contains 10 g gel...
Tk.0.55/=
A-Fenac 50 mg Tab
A-Fenac 50 TabDESCRIPTIONA-FENAC (Diclofenac Sodium) is a potent nonsteroidal, anti-inflammatory agentwith analgesic and antipyretic properties. By virtue of its analgesic, antipyreticand anti-inflammatory properties together with its excellent tolerability marks amajor advance in the treatment of rheumatic and or inflammatory conditions.Diclofenac inhibits cyclooxygenase activity with a reduction in the tissueproduction of prostaglandins.Tablet A-FENAC is enteric-coated (acid-resistant coating) with the result that the active constituent is not released until it has passed through the stomach. A-FENAC SR tablet has got many advantages. Because the frequency of drug administration is reduced, patient compliance can be improved and drug administration be made more convenient as well.COMPOSITIONTablet : Each enteric coated A-FENAC 25 tablet contains Diclofenac Sodium BP 25 mg.Each enteric coated A-FENAC 50 tablet contains Diclofenac Sodium BP 50 mg.Tablet SR : Each A-FENAC SR (sustained release) tablet contains Diclofenac Sodium BP 100 mg.Injection : Each 3 ml ampoule of A-FENAC injection contains 75 mg Diclofenac Sodium BP.Suppository : A-Fenac 12.5 : Each suppository contains declofenac sodium BP 12.5 mg.A-Fenac 50 : Each suppository contains diclofenac sodium BP 50 mg.A-FENAC Gel : Each 100 g A-FENAC Gel contains Diclofenac Diethylamine BP1.16 g equivalent to Diclofenac Sodium 1 g.INDICATIONSA-FENAC is indicated in the following cases : Rheumatoid arthritis, osteoarthritis, low back pain, injuries and manifestations of soft tissue rheumatism, ankylosing spondylitis, acute gout, control of pain & inflammation in orthopaedic, dental & other minor surgery, juvenile rheumatoid arthritis, postoperative pain, renal colic & other musculoskeletal disorders.DOSAGE & ADMINISTRATIONUsual dosing information : Tablet A-FENAC should be taken with water during or immediately after meals. Antacid should not be taken within 1-2 hours aftertaking tablet A-FENAC.Usual adult dose :A-FENAC Tablet : In adults, the initial dose is 25-50 mg three times a day, depending on the severity of the condition.A-FENAC SR Tablet : 75-150 mg once daily.Injection : For adults the usual dose is 1 ampoule daily. In serious cases this dose may be increased up to 2 ampoules daily.Suppository :Adult : 75-150 mg daily in divided doses.Children (1-12 years) : 1-3 mg/kg daily in divided dosesGel :Adult (>12 years) : A small amount (2-4 g) of A-FENAC Gel should be applied 3- 4 times daily to the affected area and rubbed lightly. Treatment is dependent on the size of the affected area. A-FENAC Gel may also be given in addition to further treatment with other dosage forms of Diclofenac.OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONA-FENAC is contraindicated in peptic ulcer, previous sensitivity to Diclofenac Sodium and in asthmatic patients in whom attacks of asthma, urticaria or acute rhinitis are precipitated by Aspirin or other nonsteroidal anti-inflammatory agents with prostaglandin synthesis inhibiting activity.SIDE EFFECTSOccasional gastrointestinal disorders, headache, dizziness or vertigo, rash, elevation of SGOT/SGPT, rare peptic ulcer, gastro-intestinal bleeding, hepatitis, hypersensitivity reactions. In isolated cases, disturbances of sensation, erythema multiforme, purpura, abnormalities of renal function, blood dyscrasias may occur. PRECAUTIONSPrecaution should be taken in patients with symptoms/history of gastro-intestinal disease, impaired hepatic, cardiac or renal function, pregnancy, porphyria and patients who are taking diuretics, anticoagulant, or antidiabetics. During prolonged treatment, periodical monitoring of liver function should be carried out and blood counts are recommended. Possibility of hypersensitivity reactions to sodium disulphite particularly in patients with asthma.SUPPLYTablet :A-FENAC 25 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC 50 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC SR : Each box contains 10x10 tablets in blisters.Injection :A-FENAC : Each box contains 2x5 ampoules in blisters.Suppository :A-FENAC 12.5 : Each box contains 2x5 suppositories in blisters.A-FENAC 50 : Each box contains 2 x 5 suppositories in blisters.Gel :A-FENAC : Each tube contains 10 g gel...
Tk.0.84/=
A-Fenac 50mg Suppository
A-Fenac 50mg suppDESCRIPTIONA-FENAC (Diclofenac Sodium) is a potent nonsteroidal, anti-inflammatory agentwith analgesic and antipyretic properties. By virtue of its analgesic, antipyreticand anti-inflammatory properties together with its excellent tolerability marks amajor advance in the treatment of rheumatic and or inflammatory conditions.Diclofenac inhibits cyclooxygenase activity with a reduction in the tissueproduction of prostaglandins.Tablet A-FENAC is enteric-coated (acid-resistant coating) with the result that the active constituent is not released until it has passed through the stomach. A-FENAC SR tablet has got many advantages. Because the frequency of drug administration is reduced, patient compliance can be improved and drug administration be made more convenient as well.COMPOSITIONTablet : Each enteric coated A-FENAC 25 tablet contains Diclofenac Sodium BP 25 mg.Each enteric coated A-FENAC 50 tablet contains Diclofenac Sodium BP 50 mg.Tablet SR : Each A-FENAC SR (sustained release) tablet contains Diclofenac Sodium BP 100 mg.Injection : Each 3 ml ampoule of A-FENAC injection contains 75 mg Diclofenac Sodium BP.Suppository : A-Fenac 12.5 : Each suppository contains declofenac sodium BP 12.5 mg.A-Fenac 50 : Each suppository contains diclofenac sodium BP 50 mg.A-FENAC Gel : Each 100 g A-FENAC Gel contains Diclofenac Diethylamine BP1.16 g equivalent to Diclofenac Sodium 1 g.INDICATIONSA-FENAC is indicated in the following cases : Rheumatoid arthritis, osteoarthritis, low back pain, injuries and manifestations of soft tissue rheumatism, ankylosing spondylitis, acute gout, control of pain & inflammation in orthopaedic, dental & other minor surgery, juvenile rheumatoid arthritis, postoperative pain, renal colic & other musculoskeletal disorders.DOSAGE & ADMINISTRATIONUsual dosing information : Tablet A-FENAC should be taken with water during or immediately after meals. Antacid should not be taken within 1-2 hours aftertaking tablet A-FENAC.Usual adult dose :A-FENAC Tablet : In adults, the initial dose is 25-50 mg three times a day, depending on the severity of the condition.A-FENAC SR Tablet : 75-150 mg once daily.Injection : For adults the usual dose is 1 ampoule daily. In serious cases this dose may be increased up to 2 ampoules daily.Suppository :Adult : 75-150 mg daily in divided doses.Children (1-12 years) : 1-3 mg/kg daily in divided dosesGel :Adult (>12 years) : A small amount (2-4 g) of A-FENAC Gel should be applied 3- 4 times daily to the affected area and rubbed lightly. Treatment is dependent on the size of the affected area. A-FENAC Gel may also be given in addition to further treatment with other dosage forms of Diclofenac.OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONA-FENAC is contraindicated in peptic ulcer, previous sensitivity to Diclofenac Sodium and in asthmatic patients in whom attacks of asthma, urticaria or acute rhinitis are precipitated by Aspirin or other nonsteroidal anti-inflammatory agents with prostaglandin synthesis inhibiting activity.SIDE EFFECTSOccasional gastrointestinal disorders, headache, dizziness or vertigo, rash, elevation of SGOT/SGPT, rare peptic ulcer, gastro-intestinal bleeding, hepatitis, hypersensitivity reactions. In isolated cases, disturbances of sensation, erythema multiforme, purpura, abnormalities of renal function, blood dyscrasias may occur. PRECAUTIONSPrecaution should be taken in patients with symptoms/history of gastro-intestinal disease, impaired hepatic, cardiac or renal function, pregnancy, porphyria and patients who are taking diuretics, anticoagulant, or antidiabetics. During prolonged treatment, periodical monitoring of liver function should be carried out and blood counts are recommended. Possibility of hypersensitivity reactions to sodium disulphite particularly in patients with asthma.SUPPLYTablet :A-FENAC 25 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC 50 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC SR : Each box contains 10x10 tablets in blisters.Injection :A-FENAC : Each box contains 2x5 ampoules in blisters.Suppository :A-FENAC 12.5 : Each box contains 2x5 suppositories in blisters.A-FENAC 50 : Each box contains 2 x 5 suppositories in blisters.Gel :A-FENAC : Each tube contains 10 g gel...
Tk.14.10/=
A-Fenac K 50 mg Tablet
A-Fenac K 50DESCRIPTIONA-FENAC K (Diclofenac Potassium) has a rapid onset of action, which makes it particularly suitable for the treatment of acute painful and inflammatory conditions. Inhibition of prostaglandin biosynthesis is considered to be fundamental to its mechanism of action. Diclofenac is rapidly and completely absorbed from A-FENAC K tablets. The absorption sets in immediately after administration.COMPOSITIONTablet : Each film-coated tablet contains Diclofenac Potassium INN 50 mg.INDICATIONSShort term treatment in the following acute conditions:• Post-traumatic pain, inflammation and swelling e.g., due to sprains.• Post-operative pain, inflammation and swelling, e.g., following dental or orthopaedic surgery.• Painful and/or inflammatory conditions in gynaecology, e.g., primary dysmenorrhoea.l• Painful syndromes of the vertebral column.• Non articular rheumatism.As an adjuvant in several painful inflammatory infections of the ear, nose or throat :• Pharyngotonsillitis.• Otitis media.DOSAGE AND ADMINISTRATIONAdults : The recommended initial daily dosage is 100-150 mg daily in 2-3 divided doses. In milder cases as well as for patients over 14 years 75-100 mg daily in 2-3 divided doses. In dysmenorrhoea the daily dosage should be individually adjusted and is generally 50- 150 mg. Children : It is not recommended for use in children. OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSOccasional epigastric pain, other gastrointestinal disorders such as nausea, vomiting, diarrhoea, abdominal cramps, dyspepsia, flatulence, anorexia etc. Occasional CNS problems such as headache, dizziness, vertigo etc.CONTRAINDICATIONSGastric or intestinal ulcer. Known hypersensitivity to the active substance or the excipients. Like other NSAIDs, Diclofenac Potassium is also contraindicated in active or suspected peptic ulcer or gastro-intestinal bleeding. Asthmatic patients in whom attacks of asthma, urticaria or acute rhinitis are precipitated by acetylsalicylic acid or other nonsteroidal anti-inflammatory agents with possessing prosta-glandin synthetase inhibiting activity.PRECAUTIONSSymptoms or history of gastro-intestinal disease, impaired hepatic, cardiac or renal function. Use with caution in elderly patients.SUPPLYTablet : Each box contains 5 x 10 tablets in blisters...
Tk.3.01/=
A-Fenac SR Tablet 100 mg , 1 strip
A-Fenac SRDESCRIPTIONA-FENAC (Diclofenac Sodium) is a potent nonsteroidal, anti-inflammatory agentwith analgesic and antipyretic properties. By virtue of its analgesic, antipyreticand anti-inflammatory properties together with its excellent tolerability marks amajor advance in the treatment of rheumatic and or inflammatory conditions.Diclofenac inhibits cyclooxygenase activity with a reduction in the tissueproduction of prostaglandins.Tablet A-FENAC is enteric-coated (acid-resistant coating) with the result that the active constituent is not released until it has passed through the stomach. A-FENAC SR tablet has got many advantages. Because the frequency of drug administration is reduced, patient compliance can be improved and drug administration be made more convenient as well.COMPOSITIONTablet : Each enteric coated A-FENAC 25 tablet contains Diclofenac Sodium BP 25 mg.Each enteric coated A-FENAC 50 tablet contains Diclofenac Sodium BP 50 mg.Tablet SR : Each A-FENAC SR (sustained release) tablet contains Diclofenac Sodium BP 100 mg.Injection : Each 3 ml ampoule of A-FENAC injection contains 75 mg Diclofenac Sodium BP.Suppository : A-Fenac 12.5 : Each suppository contains declofenac sodium BP 12.5 mg.A-Fenac 50 : Each suppository contains diclofenac sodium BP 50 mg.A-FENAC Gel : Each 100 g A-FENAC Gel contains Diclofenac Diethylamine BP1.16 g equivalent to Diclofenac Sodium 1 g.INDICATIONSA-FENAC is indicated in the following cases : Rheumatoid arthritis, osteoarthritis, low back pain, injuries and manifestations of soft tissue rheumatism, ankylosing spondylitis, acute gout, control of pain & inflammation in orthopaedic, dental & other minor surgery, juvenile rheumatoid arthritis, postoperative pain, renal colic & other musculoskeletal disorders.DOSAGE & ADMINISTRATIONUsual dosing information : Tablet A-FENAC should be taken with water during or immediately after meals. Antacid should not be taken within 1-2 hours aftertaking tablet A-FENAC.Usual adult dose :A-FENAC Tablet : In adults, the initial dose is 25-50 mg three times a day, depending on the severity of the condition.A-FENAC SR Tablet : 75-150 mg once daily.Injection : For adults the usual dose is 1 ampoule daily. In serious cases this dose may be increased up to 2 ampoules daily.Suppository :Adult : 75-150 mg daily in divided doses.Children (1-12 years) : 1-3 mg/kg daily in divided dosesGel :Adult (>12 years) : A small amount (2-4 g) of A-FENAC Gel should be applied 3- 4 times daily to the affected area and rubbed lightly. Treatment is dependent on the size of the affected area. A-FENAC Gel may also be given in addition to further treatment with other dosage forms of Diclofenac.OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONA-FENAC is contraindicated in peptic ulcer, previous sensitivity to Diclofenac Sodium and in asthmatic patients in whom attacks of asthma, urticaria or acute rhinitis are precipitated by Aspirin or other nonsteroidal anti-inflammatory agents with prostaglandin synthesis inhibiting activity.SIDE EFFECTSOccasional gastrointestinal disorders, headache, dizziness or vertigo, rash, elevation of SGOT/SGPT, rare peptic ulcer, gastro-intestinal bleeding, hepatitis, hypersensitivity reactions. In isolated cases, disturbances of sensation, erythema multiforme, purpura, abnormalities of renal function, blood dyscrasias may occur. PRECAUTIONSPrecaution should be taken in patients with symptoms/history of gastro-intestinal disease, impaired hepatic, cardiac or renal function, pregnancy, porphyria and patients who are taking diuretics, anticoagulant, or antidiabetics. During prolonged treatment, periodical monitoring of liver function should be carried out and blood counts are recommended. Possibility of hypersensitivity reactions to sodium disulphite particularly in patients with asthma.SUPPLYTablet :A-FENAC 25 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC 50 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC SR : Each box contains 10x10 tablets in blisters.Injection :A-FENAC : Each box contains 2x5 ampoules in blisters.Suppository :A-FENAC 12.5 : Each box contains 2x5 suppositories in blisters.A-FENAC 50 : Each box contains 2 x 5 suppositories in blisters.Gel :A-FENAC : Each tube contains 10 g gel...
Tk.30.10/=
A-Fenac12.5mg suppositore
A-Fenac12.5mg suppositoreDESCRIPTIONA-FENAC (Diclofenac Sodium) is a potent nonsteroidal, anti-inflammatory agentwith analgesic and antipyretic properties. By virtue of its analgesic, antipyreticand anti-inflammatory properties together with its excellent tolerability marks amajor advance in the treatment of rheumatic and or inflammatory conditions.Diclofenac inhibits cyclooxygenase activity with a reduction in the tissueproduction of prostaglandins.Tablet A-FENAC is enteric-coated (acid-resistant coating) with the result that the active constituent is not released until it has passed through the stomach. A-FENAC SR tablet has got many advantages. Because the frequency of drug administration is reduced, patient compliance can be improved and drug administration be made more convenient as well.COMPOSITIONTablet : Each enteric coated A-FENAC 25 tablet contains Diclofenac Sodium BP 25 mg.Each enteric coated A-FENAC 50 tablet contains Diclofenac Sodium BP 50 mg.Tablet SR : Each A-FENAC SR (sustained release) tablet contains Diclofenac Sodium BP 100 mg.Injection : Each 3 ml ampoule of A-FENAC injection contains 75 mg Diclofenac Sodium BP.Suppository : A-Fenac 12.5 : Each suppository contains declofenac sodium BP 12.5 mg.A-Fenac 50 : Each suppository contains diclofenac sodium BP 50 mg.A-FENAC Gel : Each 100 g A-FENAC Gel contains Diclofenac Diethylamine BP1.16 g equivalent to Diclofenac Sodium 1 g.INDICATIONSA-FENAC is indicated in the following cases : Rheumatoid arthritis, osteoarthritis, low back pain, injuries and manifestations of soft tissue rheumatism, ankylosing spondylitis, acute gout, control of pain & inflammation in orthopaedic, dental & other minor surgery, juvenile rheumatoid arthritis, postoperative pain, renal colic & other musculoskeletal disorders.DOSAGE & ADMINISTRATIONUsual dosing information : Tablet A-FENAC should be taken with water during or immediately after meals. Antacid should not be taken within 1-2 hours aftertaking tablet A-FENAC.Usual adult dose :A-FENAC Tablet : In adults, the initial dose is 25-50 mg three times a day, depending on the severity of the condition.A-FENAC SR Tablet : 75-150 mg once daily.Injection : For adults the usual dose is 1 ampoule daily. In serious cases this dose may be increased up to 2 ampoules daily.Suppository :Adult : 75-150 mg daily in divided doses.Children (1-12 years) : 1-3 mg/kg daily in divided dosesGel :Adult (>12 years) : A small amount (2-4 g) of A-FENAC Gel should be applied 3- 4 times daily to the affected area and rubbed lightly. Treatment is dependent on the size of the affected area. A-FENAC Gel may also be given in addition to further treatment with other dosage forms of Diclofenac.OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONA-FENAC is contraindicated in peptic ulcer, previous sensitivity to Diclofenac Sodium and in asthmatic patients in whom attacks of asthma, urticaria or acute rhinitis are precipitated by Aspirin or other nonsteroidal anti-inflammatory agents with prostaglandin synthesis inhibiting activity.SIDE EFFECTSOccasional gastrointestinal disorders, headache, dizziness or vertigo, rash, elevation of SGOT/SGPT, rare peptic ulcer, gastro-intestinal bleeding, hepatitis, hypersensitivity reactions. In isolated cases, disturbances of sensation, erythema multiforme, purpura, abnormalities of renal function, blood dyscrasias may occur. PRECAUTIONSPrecaution should be taken in patients with symptoms/history of gastro-intestinal disease, impaired hepatic, cardiac or renal function, pregnancy, porphyria and patients who are taking diuretics, anticoagulant, or antidiabetics. During prolonged treatment, periodical monitoring of liver function should be carried out and blood counts are recommended. Possibility of hypersensitivity reactions to sodium disulphite particularly in patients with asthma.SUPPLYTablet :A-FENAC 25 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC 50 : Each box contains 10x10 enteric coated tablets in blisters.A-FENAC SR : Each box contains 10x10 tablets in blisters.Injection :A-FENAC : Each box contains 2x5 ampoules in blisters.Suppository :A-FENAC 12.5 : Each box contains 2x5 suppositories in blisters.A-FENAC 50 : Each box contains 2 x 5 suppositories in blisters.Gel :A-FENAC : Each tube contains 10 g gel...
Tk.8.07/=
A-Migel 30 gm Gel
A-Migel 30 gm GelDescriptionMiconazole is a synthetic imidazole anti-fungal agent with a broadspectrum of activity against pathogenic fungi (including yeast and dermatophytes) and gram-positive bacteria (Staphylococcus and Streptococcus spp). It may act by interfering with the permeability of the fungal cell membranes. Miconazole oral gel is incompletely absorbed from the gastrointestinal tract. Miconazole is inactivated in the body and 10-20% of an oral dose is excreted in the urine.CompositionEach gram oral gel contains 20 mg Miconazole USP.IndicationOral treatment and prevention of fungal infections of the oropharynx and gastrointestinal tract.Dosage and AdministrationFor oral administration : Dosage is based on 15 mg/kg/day after meal. Adults : 1-2 tea-spoonfuls of gel four times daily.Children aged 6 years and over : One tea-spoonful of gel four times daily.Children aged 2-6 years : One tea-spoonful of gel twice daily. Infants under 2 years : Half tea-spoonful of gel twice daily. For localised lesions of the mouth, a small amount of A-Migel oral gel may be applied directly to the affected area with a clean finger 2-4 times daily. For topical treatment of the oropharynx, the gel should be kept in the mouth for as long as possible. Treatment should be continued for up to 2 days after the symptoms have cleared. For oral candidiasis, dental prostheses should be removed at night and brushed with the gel.OR AS DIRECTED BY THE PHYSICIANSide effectsOccasionally, nausea and vomiting have been reported and with long term treatment, diarrhoea is also reported.ContraindicationsMiconazole is contraindicated in patients with known hypersensitivity to the active drug and imidazole group.PrecautionThe concomitant use of Miconazole with anti-coagulant, anti-epileptic and anti-diabetic drugs increases the affectivity of these drugs. So dosage of Miconazole should be revised.Use in Pregnancy & LactationIn animals Miconazole has shown no teratogenic effects but is foetotoxic at high oral doses. However, as with other imidazoles, Miconazole Oral Gel should be avoided in pregnant women if possible. The potential hazards should be balanced against the possible benefits. It is not known whether Miconazole is excreted in human milk. Caution should be exercised when prescribing Miconazole Oral Gel to nursing mothers.Over dosageIn general, Miconazole is not highly toxic. In the event of accidental over dosage, vomiting and diarrhoea may occur.SupplyOral Gel : Each carton contains 15 gm oral gel in tube and a spoon...
Tk.90.00/=
A-Phenicol Drop 10 ml drop
A-Phenicol Drop 10 ml dropDESCRIPTIONChloramphenicol is a broad spectrum antibiotic, isolated in 1947 from streptomyces venezuelae. It is primarily bacteriostatic and acts by inhibition of protein synthesis. It has been noted that chloramphenicol is found in measurable amounts in the aqueous humor following local application to the eye. Development of resistance to Chloramphenicol is minimum for staphylococci and many other species of bacteria.COMPOSITIONEYE OINTMENT : Each gm contains 10 mg of Chloramphenicol BP in a special base. It is a sterile eye ointment.EYE/EAR DROPS : Each ml eye/ear drops contains Chloramphenicol BP 5 mg. It is a sterile eye / ear drops.INDICATIONSA-PHENICOL is indicated in surface ocular infections involving the conjunctiva and/or cornea caused by Chloramphenicol susceptible organisms. A-PHENICOL is also active against common bacterial pathogens, E.coli, Klebsiella, Niesseria sp., H.influenzae, Enterobacter sp., Staphylococcus aureus and Streptococcus pneumoniae.A-PHENICOL is also indicated in ear canal infection.DOSAGE AND ADMINISTRATIONA-PHENICOL Eye OintmentA PHENICOL eye ointment should be used every three hours. Administration should be continued day and night for the first 48 hours after which the interval between application may be increased and continued for at least 2 days after the eye appears normal.A-PHENICOL Eye/Ear DropsFor eye : 2 drops of solution every 1 hour, until condition improves or instill 4 times daily depending on severity of infection. For ear : (Adult & Children) : 2 or 3 drops in the affected ear 2-3 times daily. OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONSChloramphenicol is contraindicated in patients sensitive to any of its components.PRECAUTIONSOphthalmic ointments may retard corneal wound healing. So patients with corneal disease should take precautions while using this medicine.SUPPLYA-PHENICOL Eye Ointment : A-PHENICOL Eye Ointment is supplied in 5 gmcollapsible tube.A-PHENICOL Eye/Ear Drops : A-PHENICOL Eye/Ear Drops is supplied in 10 mlplastic bottle with dropper...
Tk.34.50/=
A-Phenicol Eye Ointment 5g
A-Phenicol Eye Ointment 5gDESCRIPTIONChloramphenicol is a broad spectrum antibiotic, isolated in 1947 from streptomyces venezuelae. It is primarily bacteriostatic and acts by inhibition of protein synthesis. It has been noted that chloramphenicol is found in measurable amounts in the aqueous humor following local application to the eye. Development of resistance to Chloramphenicol is minimum for staphylococci and many other species of bacteria.COMPOSITIONEYE OINTMENT : Each gm contains 10 mg of Chloramphenicol BP in a special base. It is a sterile eye ointment.EYE/EAR DROPS : Each ml eye/ear drops contains Chloramphenicol BP 5 mg. It is a sterile eye / ear drops.INDICATIONSA-PHENICOL is indicated in surface ocular infections involving the conjunctiva and/or cornea caused by Chloramphenicol susceptible organisms. A-PHENICOL is also active against common bacterial pathogens, E.coli, Klebsiella, Niesseria sp., H.influenzae, Enterobacter sp., Staphylococcus aureus and Streptococcus pneumoniae.A-PHENICOL is also indicated in ear canal infection.DOSAGE AND ADMINISTRATIONA-PHENICOL Eye OintmentA PHENICOL eye ointment should be used every three hours. Administration should be continued day and night for the first 48 hours after which the interval between application may be increased and continued for at least 2 days after the eye appears normal.A-PHENICOL Eye/Ear DropsFor eye : 2 drops of solution every 1 hour, until condition improves or instill 4 times daily depending on severity of infection. For ear : (Adult & Children) : 2 or 3 drops in the affected ear 2-3 times daily. OR AS DIRECTED BY THE PHYSICIAN.CONTRAINDICATIONSChloramphenicol is contraindicated in patients sensitive to any of its components.PRECAUTIONSOphthalmic ointments may retard corneal wound healing. So patients with corneal disease should take precautions while using this medicine.SUPPLYA-PHENICOL Eye Ointment : A-PHENICOL Eye Ointment is supplied in 5 gmcollapsible tube.A-PHENICOL Eye/Ear Drops : A-PHENICOL Eye/Ear Drops is supplied in 10 mlplastic bottle with dropper...
Tk.11.70/=
A-Phenicol-D Ophthalmic Solution 5 ml drop
A-Phenicol-D Ophthalmic Solution 5 ml dropIndications: Acute purulent conjunctivitis; fresh inflammation of the superficial and deeper corneal layers and corneal ulceration. Keratitis disciformis and the more deep-seated forms of post-herpetic keratitis. Allergic conjunctivitis, allergic blepharitis. Acute and chronic iritis and iridocyclitis.Dosage and AdministrationOne drop into the lower eyelid of the infected eye(s), 1-4 times daily. In acute cases 1 drop every hour. OR AS DIRECTED BY THE PHYSICIAN.Side Effects: Local use of dexamethasone over a prolonged period may lead in some cases to secondary glaucoma and the development of complicated cataract.Precautions and Contraindications: It must be used under strict medical supervision because of the possibility of inducing corneal abscess, fungal keratopathy or glaucoma. The patient should be referred to an ophthalmologist if the eye has not responded within 48 hours.Use in Pregnancy & Lactation: The safety of this combination during pregnancy has not yet been established. It is not known whether ingredients of this ophthalmic preparation is excreted in human milk. Therefore caution should be observed when it is administered to a nursing mother.Drug Interactions: Specific drug interaction studies have not been conducted with this combination.Supply: Each pack contains 5 ml sterile eye drops in plastic dropper bottle...
Tk.70.21/=
A-Zyme 325 mg Tablet, 1 strip
A-Zyme 325 mg Tablet, 1 stripDESCRIPTIONA-Zyme (Pancreatin) is a preparation of Pancreatin, an extract from mammalian pancreas containing enzymes with Amylase, Protease and Lipase activity. It is designed to disintegrate in the alkaline medium of the duodenum where it releases the active enzyme components of Pancreatin (Amylase, Protease and Lipase). Amylase hydrolyzes dietary starch to yield maltose, maltoriose and adextrin. Protease cleaves peptide bonds in the center of proteins and polypeptides and forms amino acids and oligopeptides. Lipase hydrolyzes dietary triglycerides forming two molecules of fatty acid and a molecule of betamonoglyceride. It converts not less than 25 times its weight of starch into soluble carbohydrates and not less than 25 times its weight of casein into proteoses within 5 mins. (equivalent to 150 times in 30 mins).COMPOSITIONEach enteric-film-coated tablet contains 325 mg of Pancreatin BP that provides not less than the following enzymatic activityAmylase 7800 units Protease 455 units Lipase 6500 unitsINDICATIONSA-Zyme is employed for the treatment of patients with● Chronic pancreatitis● Cystic fibrosis/Mucoviscidosis● Following partial or complete pancreatectomy● Total gastrectomy● Steatorrhea● Somatostatinoma● Celiac disease and● Other conditions associated with pancreatic insufficiency.DOSAGE AND ADMINISTRATION2-3 tablets to be swallowed whole with little water immediately after or during meal.OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSThe most frequent side effects are gastrointestinal including nausea, vomiting and abdominal discomfort. Buccal and perianal soreness may occur, particularly in infants. Hypersensitivity reactions manifested by sneezing, lacrimation or skin rashes have been reported.CONTRAINDICATIONSPancreatin is contraindicated in patients with known hypersensitivity to the drug.PRECAUTIONSPatients known to be allergic to animal protein should be treated with caution.USE IN PREGNANCY AND LACTATIONPancreatin should be given to a pregnant woman only if clearly needed. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Pancreatin is administered to a nursing mother.DRUG INTERACTIONSAlkaline media will rupture the enteric coating. As such to prevent bursting out of the content in the stomach Pancreatin should not be used concurrently with antacid.OVERDOSAGEExcessive dosage may produce a laxative effect. Systemic toxicity does not occur. Very high dosage may cause hyperuricaemia and hyperuricosuria.SUPPLYEach box contains 10 X 10 tablets in strips...
Tk.35.10/=
