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A-Fenac 50 mg Tab

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/=

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A-Fenac 50mg Suppository

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/=

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A-Fenac SR Tablet 100 mg , 1 strip

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/=

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A-Fenac12.5mg suppositore

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/=

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Miclofenac 50 mg tablet

Miclofenac 50 mg tablet

Indication:Osteoarthritis or rheumatoid arthritis in patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications.Dosage & Administration:Osteoarthritis: Miclofenac® 50 TID. For patients who experience intolerance, Miclofenac® 50 BID or Miclofenac® 75 BID can be used. Rheumatoid Arthritis: Miclofenac® 50 TID or QID. For patients who experience intolerance, Miclofenac® 50 BID or Miclofenac® 75 BID can be used.Preparation:Miclofenac® 50: Box containing 3 x 10's tablet in blister pack.Miclofenac® 75: Box containing 3 x 10's tablet in blister pack...

Tk.10.07/=

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Miclofenac 75 mg Tablet

Miclofenac 75 mg Tablet

Indication:Osteoarthritis or rheumatoid arthritis in patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications.Dosage & Administration:Osteoarthritis: Miclofenac® 50 TID. For patients who experience intolerance, Miclofenac® 50 BID or Miclofenac® 75 BID can be used. Rheumatoid Arthritis: Miclofenac® 50 TID or QID. For patients who experience intolerance, Miclofenac® 50 BID or Miclofenac® 75 BID can be used.Preparation:Miclofenac® 50: Box containing 3 x 10's tablet in blister pack.Miclofenac® 75: Box containing 3 x 10's tablet in blister pack...

Tk.11.07/=

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Ultrafen 100 SR

Ultrafen 100 SR

1. What Ultrafen® is and what it is used for?Ultrafen® is a preparation of Diclofenac is a non-steroidal anti-inflammatory agent with marked analgesic, anti-inflammatory and antipyretic properties. Ultrafen® is indicated for rheumatoid arthritis, osteoarthritis, low back pain and other acute musculo-skeletal disorders such as frozen shoulder, tendinitis, tenosynovitis, bursitis, sprain, strain and dislocation, ankylosing spondylitis, acute gout, pain in orthopaedics, dental and other minor surgery. 2. Before you take Ultrafen® Do not take this medicine and tell your doctor if: Before taking Ultrafen®, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies.Ultrafen® should not be prescribed to pregnant women unless there is compelling reason for doing so. Patients with a history of peptic ulcer, haematemesis, melaena, bleeding diathesis or with severe hepatic or renal insufficiency, should be kept under close surveillance. If abnormal liver function tests persist or worsen, clinical signs and symptoms consistent with liver disease or if other manifestations occur (eosinophilia, rash), Ultrafen® should be discontinued. Use of Ultrafen® in patients with hepatic porphyria may trigger an attack. Take special care with Ultrafen® Check with your doctor before taking this medicine if: Ultrafen® should not be given in patients with previous hypersensitivity to Diclofenac, asthmatic patients and in whom attacks of asthma, urticarial or acute rhinitis are precipitated by Aspirin or other NSAIDs. Taking other medicines Lithium and digoxin: Diclofenac may increase plasma concentrations of lithium and digoxin. Anticoagulants: There are isolated reports of an increased risk of haemorrhage with the combined use of diclofenac and anticoagulant therapy, although clinical investigations do not appear to indicate any influence on anticoagulant effect. Antidiabetic agents: Clinical studies have shown that diclofenac can be given together with oral antidiabetic agents without influencing their clinical effects. Cyclosporin: Cases of nephrotoxicity have been reported in patients receiving cyclosporin and diclofenac concomitantly. Methotrexate: Cases of serious toxicity have been reported when methotrexate and NSAIDs are given within 24 hours with each other. Quinolone antimicrobials: Convulsions may occur due to an interaction between quinolones and NSAIDs. Therefore, caution should be exercised when considering Concomitant therapy of NSAID and quinolones. Other NSAIDs and steroids: Co-administration of diclofenac with other systemic NSAIDs and steroids may increase the frequency of unwanted effects. With aspirin, the plasma levels of each is lowered, although no clinical significance is known. Diuretics: Various NSAIDs are liable to inhibit the activity of diuretics. Concomitant treatment with potassium‐sparing diuretics may be associated with increased serum potassium levels. So, serum potassium should be monitored. Pregnancy and breast-feeding Diclofenac should not be prescribed during pregnancy, unless there are compelling reasons for doing so. The lowest effective dosage should be used. 3. How to take Ultrafen®? Enteric coated tablet: A total of 75-150 mg daily given in two or three divided doses. Sustained release tablets: One tablet daily, taken whole with liquid, preferably during meal Suppositories: 75-150 mg daily in divided doses. If you forget to take Ultrafen® If 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 Ultrafen® Do not stop taking this medicine without talking to your doctor. You should not stop taking Ultrafen® just because you feel better. This is because the problem may come back or get worse again. If you have any further questions on the use of this product, ask your doctor or pharmacist. 4. Possible side effects Like all medicines, Ultrafen® can cause side effects, although not everybody gets them. Epigastric pain, nausea and diarrhoea, headache and slight dizziness may be complained by some patients. These are often transient, disappearing with continuation of medication 5. How to store Ultrafen®? Store in a cool and dry place, away from light. Keep out of reach of children Ultrafen Prescribing InformationLocated in: Muscloskeletal..

Tk.3.00/=

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Ultrafen PLUS tablet

Ultrafen PLUS tablet

1. What Ultrafen® Plus is and what it is used for?Ultrafen® Plus is a combination product containing Diclofenac Sodium, a nonsteroidal anti-inflammatory drug (NSAID) with analgesic properties, and Misoprostol, a gastrointestinal (GI) mucosal protective prostaglandin E1 analogue. This combination product is indicated for the treatment of signs and symptoms of osteoarthritis or rheumatoid arthritis in patients at high risk of developing NSAID induced gastric and duodenal ulcers and their complications.2. Before you take Ultrafen® Plus Do not take this medicine and tell your doctor if: Before taking Ultrafen® Plus, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. Diclofenac Sodium and Misoprostol combination is used cautiously in patients with an underlying condition such as inflammatory bowel disease, or those in whom dehydration should be monitored carefully. Take special care with Ultrafen® Plus Check with your doctor before taking this medicine if: Ultrafen® Plus is contraindicated in pregnant women because of the abortifacient property of Misoprostol. The drug is contraindicated in patients with hypersensitivity to any of its ingredients. Taking other medicines Aspirin: Concomitant administration with aspirin is not recommended because Diclofenac Sodium is displaced from its binding sites by Aspirin, resulting in lower plasma concentrations, peak plasma levels and AUC values. Digoxin: Elevated digoxin levels have been reported in patients receiving digoxin and Diclofenac Sodium concomitantly. Antihypertensives: NSAIDs can inhibit the activity of antihypertensives, including ACE inhibitors. Thus, caution should be taken when administering it with such agents. Warfarin: The effects of warfarin and NSAIDs on GI bleeding are synergistic, such that users of both drugs together have a risk of serious bleeding greater than users of either drug alone. Oral hypoglycaemics: Diclofenac Sodium does not alter glucose metabolism in healthy people nor it alters the effects of oral hypoglycaemics. There are rare reports, however, from marketing experience, of changes in effects of insulin or oral hypoglycaemics in the presence of Diclofenac Sodium that necessitated change in the doses of such agents. Both hypoand hyperglycaemic effects have been reported. A direct causal relationship has not been established, but physicians should consider the possibility that Diclofenac Sodium may alter a diabetic patient’s response to insulin or oral hypoglycaemics. Antacids: Antacids reduce the bioavailability of Misoprostol acid and may delay absorption of Diclofenac Sodium. Magnesium containing antacidsexacerbate Misoprostol associated diarrhoea. Thus, it is not recommended that it be coadministered with antacids. Diuretics: The Diclofenac Sodium component like other NSAIDs, can inhibit the activity of diuretics. Concomitant therapy with potassium sparing diuretics may be associated with increased serum potassium levels Pregnancy and breast-feeding Ultrafen® Plus is contraindicated in pregnant women because of the abortifacient property of Misoprostol. Because of the potential for serious adverse reactions in nursing infants, Diclofenac Sodium and Misoprostol combination is not recommended for use by nursing mothers. 3. How to take Ultrafen® Plus? Osteoarthritis: The recommended dosage for maximal GI mucosal protection is Diclofenac Sodium 50 mg plus Misoprostol 200 mg tid. For patients who experience intolerance, Diclofenac Sodium 75 mg plus Misoprostol 200mg bid or Diclofenac Sodium 50 mg plus Misoprostol 200 mg bid can be used. Rheumatoid arthritis: The recommended dosage is Diclofenac Sodium 50 mg plus Misoprostol 200 mg tid or qid. For patients who experience intolerance, Diclofenac Sodium 75 mg plus Misoprostol 200 mg bid or Diclofenac Sodium 50 mg plus Misoprostol 200 mg bid can be used. If you forget to take Ultrafen® Plus If 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 Ultrafen® Plus Do not stop taking this medicine without talking to your doctor. You should not stop taking Ultrafen® Plus just because you feel better. This is because the problem may come back or get worse again. If you have any further questions on the use of this product, ask your doctor or pharmacist. 4. Possible side effects Like all medicines, Ultrafen® Plus can cause side effects, although not everybody gets them. The most common reported side effects are abdominal pain, diarrhoea and other GI symptoms. Diarrhoea and abdominal pain developed early in the course of therapy, and were usually self limited (resolved after 2 to 7 days). Rare instances of profound diarrhoea leading to severe dehydration have been reported in patients receiving Misoprostol. 5. How to store Ultrafen® Plus? Store in a cool and dry place, away fr..

Tk.10.00/=

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VOLINAC 50 gm Gel

VOLINAC 50 gm Gel

IndicationsIndicated for the quick relief from pain, swelling and inflammation due to musculo-skeletal disorders such as sprains, strains, tendinitis, bursitis, hands, neck & shoulder pain, sciatica, muscle stiffness, joint pain, back ache and lumbago.Therapeutic ClassNon-steroidal Anti-inflammatory Drugs (NSAIDs)PharmacologyDiclofenac Diethylamine is systemically absorbed through the skin; it inhibits the enzyme cyclooxygenase, thus reducing the formation of PGE2. Moreover, it also increases the uptake of Arachidonic acid into the cellullar pool. Menthol is a vasodilator. It dilates the blood vessels, produces a feeling of coolness and produces analgesia. Methyl salicylate is a known anti-inflammatory agent.Dosage & AdministrationApproximately one-inch band of gel should be applied to the affected site three to four times daily with rubbing till the film disappears.ContraindicationsKnown hypersensitivity to any part of the preparation.Side EffectsUsually well tolerated. Extremely low frequency of hypersensitivity reactions.Pregnancy & LactationThe safety of this gel has not been established during pregnancy. There are no well-controlled studies of diclofenac in pregnant women.Precautions & WarningsFor external use only. Avoid contact with the eyes. Stop use and ask a doctor if condition worsens or does not improve within 7 days. Keep out of the reach of children. If swallowed, get medical help or contact a poison control center right away.Use in Special PopulationsSafety and effectiveness in pediatric patients have not been established.Storage ConditionsStore below 30° c. Do not freeze. Keep out of reach of children. Close cap tightly after each application...

Tk.100.00/=

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