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Ace Plus Tablet

Ace Plus Tablet

Indication: Fever, headache, migraine, muscle ache, backache, toothache & menstrual pain.Dosage & Administration:Adults: 1-2 tablets every 4-6 hours. Maximum dose: 8 tablets daily. Not recommended for children below 12 years.Preparation: Each box contains 200 tablets of Paracetamol 500 mg & Caffeine 65 mg in a blister pack...

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Fastdol 325/37.5 mg Tablet

Fastdol 325/37.5 mg Tablet

Fastdol 325 / 37.5 mg TabletDESCRIPTIONTramadol Hydrochloride is an opioid analgesic that acts on the central nervous system. It is a pure non selective agonists of the mu, delta, and kappa opioid receptors with a higher affinity for the mu receptors. Unlike morphine, a broad range of analgesic doses of Tramadol Hydrochloride has no respiratory depressant effect. The precise mechanism of the analgesic properties of paracetamol is unknown and may involve central and peripheral effects.COMPOSITIONEach film -coated tablet contains Paracetamol BP 325 mg & Tramadol Hydrochloride BP 37.5 mg.INDICATIONSFor the management of moderate to severe pain.DOSAGE AND ADMINISTRATIONAdultThe recommended dose is 1 or 2 tablets every 4 to 6 hours for 5 days or less.. Additional doses can be taken as needed, not exceeding 8 tablets (equivalent to 300 mg tramadol and 2600 mg paracetamol) per day.The dosing interval should not be less than six hours.ChildrenThe effective and safe use of FASTDOL has not been established in children below the age of 16 years. Treatment is therefore not recommended in this population.OR AS DIRECTED BY THE PHYSICIAN.SIDE EFFECTSThe most commonly reported undesirable effects during the clinical trials performed with the Paracetamol/TramadolHydrochloride combination were nausea, dizziness and somnolence.CONTRAINDICATIONSHypersensitivity to Tramadol Hydrochloride, paracetamol or to any of the ingredient of the medicinal product. FASTDOL should not be administered to patients who are receiving monoamine oxidase inhibitors or within two weeks of their withdrawal.PRECAUTIONSShould be used with caution in opioid dependent patients, or in patients with cranial trauma, in patients prone to convulsive disorder, biliary tract disorders, in a state of shock, in an altered state of consciousness for unknown reasons, with problems affecting the respiratory center or the respiratory function, or with an increased intracranial pressure. Paracetamol in over dosage may cause hepatic toxicity in some patients.PREGNANCY AND LACTATIONPregnancy category C. Since it is a fixed combination of active ingredients including Tramadol Hydrochloride, it should not be used during pregnancy & lactation.DRUG INTERACTIONSConcomitant administration of CYP2D6 and/or CYP3A4 inhibitors such as quinidine, fluoxetine, paroxetine. and amitriptyline (CYP2D6 inhibitors), and ketoconazole and erythromycin (CYP3A4 inhibitors), may reduce metabolic clearance of tramadol, increasing the risk for serious adverse events including seizures and serotonin syndrome.SUPPLYEach Box contains 3x10 tablets in blister strips...

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Napa 500 Tablet

Napa 500 Tablet

Napa 500 TabletWhat Napa® is and what it is used for?Napa® (Paracetamol) is a fast acting and safe analgesic with marked antipyretic property.It is recommended for the treatment of most painful and febrile conditions, such as headache, toothache, backache, rheumatic and muscle pains, dysmenorrhoea, sore throat, and for relieving the fever, aches and pains of colds and flu.Before you take Napa®Care is advised in the administration of Napa® to patients with renal or hepatic impairment. The hazard of overdose is greater in those with non-cirrhotic alcoholic liver disease.Seek advice from your doctor if you are pregnant or breastfeeding.Do not-exceed the stated dosetake other paracetamol-containing products concurrentlyConsult your doctor-if symptoms persistif your headaches become persistentif you suffer from non-serious arthritis and need to take painkillers every dayHow to take Napa®Tablet:Adults: 1-2 tablets 3-4 times dailySyrup/Suspension:Adults: 4-8 Measuring spoonful 3-4 times daily;Children: 6-12 years: 2- 4 measuring spoonful 3-4 times daily, 1-5 years: 1-2 Measuring spoonful 3-4 times daily, Up to 1 year: 1/2 -1 Measuring spoonful 3-4 times dailyPaediatric drops:Neonates & Children: 0-3 months: 0.5 ml, 4-11 months: 1ml, 12-23 months: 1.5 ml, 2-3 years: 2 ml, 4-5 years: 3 ml four times daily or as directed by physicians.Suppositories:Children: 1-5 years: 125- 250 mg, 6-12 years: 250-500 mg up to 4 times dailyPossible side effectsSide effects of paracetamol are usually mild, though haematological reactions including thrombocytopenia, leucopenia, pancytopenia, neutropenia, and agranulocytosis have been reported. Pancreatitis, skin rashes, and other allergic reactions occur occasionally.How to store Napa®Store in a cool and dry place, away from light. Keep out of the reach and sight of children. Napa Prescribing Information..

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Napa Extend tablet

Napa Extend tablet

Napa Extend tabletWhat Napa Extend is and what it is used for?Napa® Extend is the preparation of Paracetamol 665 mg extended release formulation. It is formulated by dual granulation technology. There are two types’ granules in each tablet 31% (206 mg) is in immediate release form for immediate action and 69% (459 mg) in sustain release form for continuous pain relief for 8 hours.Paracetamol 665 mg Extended Release tablet is effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. Paracetamol 665 mg Extended Release tablet also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold & flu. Reduces fever.Before you take Napa ExtendDo not take this medicine and tell your doctor if:Hypersensitivity to Paracetamol or to any of the excipients.Take special care with Napa ExtendCheck with your doctor before taking this medicine if:Paracetamol should be administered with caution to patients with hepatic or renal Dysfunction.Taking other medicinesAnticoagulant dosage may require reduction if paracetamol medication is prolonged. Paracetamol absorption from immediate release preparations is increased by drugs which increase gastric emptying, eg metoclopramide, and decreased by drugs which decrease gastric emptying, eg propantheline, antidepressants with anticholinergic properties, narcotic analgesics.Pregnancy and LactationPregnancy category: B This drug should not be used during pregnancy unless the benefit outweighs the risk.A decision should be made to discontinue breastfeeding or to not administer the drug, taking into account the importance of the drug to the mother.Warnings & PrecautionHypersensitivity Reactions: Serious hypersensitivity reactions, including anaphylactic-type reactions, some of which have been life-threatening and fatal, have been reported in patients receiving Ferric Carboxymaltose. Patients may present with shock, clinically significant hypotension, loss of consciousness, and/or collapse.How to take Napa ExtendParacetamol 665 mg Extended Release tablet are to be administered orally, with or without food. Adults and children over 12 years. Two tablets, swallowed whole, every 6 to 8 hours (maximum of 6 tablets in any 24 hours). The tablets must not be crushed.If you forget to take Napa ExtendIf you forget to take a dose, take it as soon as you remember it. If it is almost time for your next dose, do not take the missed dose. Take the next dose on time.If you stop taking Napa ExtendDo not stop taking this medicine without talking to your doctor. You should not stop taking Napa Extend just because you feel better. This is because the problem may come back or get worse again.If you have any further questions on the use of this product, ask your doctor or pharmacist.Possible side effects (Adverse effect/Side effect as short form)Like all medicines, Napa Extend can cause side effects, although not everybody gets them.Reports of adverse reactions are rare. Although the following adverse reactions have been reported, a causal relationship to the administration of paracetamol has been neither confirmed nor refuted: dyspepsia, nausea, allergic and haematological reactions.How to store Napa Extend (Storage condition)?Store in a cool and dry place and keep away from children. Napa Extend Prescribing Information..

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Napadol 325/37.5 mg tablet

Napadol 325/37.5 mg tablet

Napadol tabletWhat is NapaDol®?NapaDol® is a combination of two Paracetamol 325 mg and Tramadol 37.5 mg tablet. Tramadol Hydrochloride is an opioid analgesic that acts on the central nervous system. Tramadol is pure non selective agonists of the m, d, and k opioid receptors with a higher affinity for the m receptors. Unlike morphine, Tramadol Hydrochloride has no respiratory depressant effect. Paracetamol (acetaminophen) is a pain reliever and a fever reducer which is used to treat many conditions such as headache, muscle aches, arthritis, backache, toothaches, colds, and fevers. Combination of Paracetamol and Tramadol exerts a synergistic effect and subsides mutual side effects.When to take NapaDol®?NapaDol® is indicated for the symptomatic treatment of moderate to severe pain.How to take NapaDol®?For the management of pain, the recommended dose is 1 or 2 tablets every 4 to 6 hours as needed for pain relief up to a maximum of 8 tablets per day. The dosing interval should not be less than six hours.Who should not take NapaDol®?NapaDol® is not recommended in patients under 18 years of age. NapaDol® should not be used in patients who have hypersensitivity to Tramadol Hydrochloride, Paracetamol or to any of the excipients of the medicinal product. It is contraindicated in case of acute intoxication with alcohol, hypnotic drugs, centrally‐acting analgesics, opioids or psychotropic drugs. It should not be administered to patients who are receiving monoamine oxidase inhibitors or within two weeks of their withdrawal, who have severe hepatic impairment and epilepsy not controlled by treatment.How NapaDol® works?Tramadol in NapaDol® works by changing the way the body senses pain, meaning that Tramadol modifies the way in which the body reacts to pain. The precise mechanism of the analgesic properties of Paracetamol, the other component of NapaDol® is unknown and may involve central and peripheral effects.How supplied?Box containing 30 tablets in 3x10’s blister strips. Each film coated tablet contains Paracetamol BP 325 mg & Tramadol Hydrochloride BP 37.5 mg. NapaDol Prescribing Information..

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Resadol

Resadol

ResadolDescriptionParacetamol is a non-opiate, non-salicylate analgesic. Tramadol is a centrally acting synthetic opioid analgesic. Although its mode of action is not completely understood, from animal tests, at least two complementary mechanisms appear applicable: binding of parent and M1 metabolite to m-opioid receptors and weak inhibition of reuptake of nor-epinephrine and serotonin.Opioid activity is due to both low affinity binding of the parent compound and higher affinity binding of the O-demethylated metabolite M1 to m-opioid receptors.As some other opioid analgesics, Tramadol has been shown to inhibit reuptake of nor-epinephrine and serotonin in vitro. These mechanisms may contribute independently to the overall analgesic profile of Tramadol.IndicationsResadol tablet is indicated for the management of moderate to moderately severe pain in adults.Resadol tablet is also indicated for the short-term (five days or less) management of acute pain.Dosage & AdministrationResadol tablet can be administered without regard to food.For the management of moderate to moderately severe pain, the recommended dose is 1 or 2 tablets every 4 to 6 hours as needed for pain relief up to a maximum of 8 tablets per day.In case of short-term (five days or less) management of acute pain, the recommended dose is 2 tablets every 4 to 6 hours as needed for pain relief up to a maximum of 8 tablets per day.Pediatric & geriatric use: The safety and effectiveness of this combination preparation has not been studied in the pediatric population. In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal or cardiac function; of concomitant disease and multiple drug therapy.Use in renal disease: This combination preparation has not been studied in patients with impaired renal function. In patients with creatinine clearances of less than 30 ml/min, it is recommended that the dosing interval of this combination preparation be increased but not to exceed 2 tablets every 12 hours.Use in hepatic disease: This combination preparation has not been studied in patients with impaired hepatic function. The use of this combination preparation in patients with hepatic impairment is not recommended.Side EffectsThe following adverse reactions may happen to this therapy: asthenia, fatigue, hot flushes, dizziness, headache, tremor, abdominal pain, constipation, diarrhea, dyspepsia, dry mouth, nausea, vomiting, anorexia, anxiety, confusion, euphoria, insomnia, nervousness, somnolence pruritus, rash, increased sweating etc.PrecautionsThis combination preparation may impair mental or physical abilities required for the performance of potentially hazardous tasks such as driving a car or operating machinery.This combination preparation should not be taken with alcohol containing beverages.The patient should be instructed not to take this combination preparation in combination with other Tramadol or Paracetamol-containing products, including over-the-counter preparations.This combination preparation should be used with caution when taking medications such as tranquilizers, hypnotics or other opiate containing analgesics.Use in Pregnancy & LactationPregnancy Category CThere are no adequate and well-controlled studies in pregnant women. This combination preparation should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.This combination preparation is not recommended for obstetrical preoperative medication or for post-delivery analgesia in nursing mothers because its safety in infants and newborns has not been studied.StorageStore in cool and dry place. Do not freeze.Commercial PackResadol Tablet: Each commercial box contains 3 alu-pvdc blister strips of 10 tablets...

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Reset Plus Tablet

Reset Plus Tablet

Reset Plus Tablet DescriptionReset Plus (Paracetamol & Caffeine) is a fast acting and safe analgesic with marked antipyretic property. It is specially suitable for patients who, for any reason, can not tolerate aspirin or other analgesics. The presence of Caffeine increases the effectiveness of Paracetamol.IndicationsThe indications of Reset Plus are as follows :* Headache* Migraine* Toothache* Neuralgia* Feverishness* Period pain* Sore throat* Backache* Helps reduce temperature* Aches and pain of colds and fluDosage & AdministrationAdult: 1 - 2 tablets every 4 to 6 hours. Maximum dose 4 gm (8 tablets) daily.Side EffectsSide effects of paracetamol are usually mild, though haematological reactions including thrombocytopenia, leukopenia, pancytopenia, neutropenia, and agranulocytosis have been reported. Pancreatitis, skin rashes, and other allergic reactions occur occasionally.PrecautionsParacetamol & Caffeine should be given cautiously in the following cases: In patients with hepatic or renal failure, in patients taking other hepatotoxic medication. Prolonged use of the drug without consulting a physician should be avoided.Use in Pregnancy & LactationPregnant mothers should consult with doctors before taking Paracetamol & Caffeine. Paracetamol & Caffeine can be taken whilst breast feeding.Over DoseSymptoms of Paracetamol overdose in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain. Liver damage may become apparent 12 to 40 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur.Commercial PackReset Plus: Box containing 10 blister strips of 10 tablets...

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