Diclofenac sodium and misoprostol delayed-release tablets are indicated for treatment of the signs and symptoms of osteoarthritis or rheumatoid arthritis in adult patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications. For a list of factors that may increase the risk of NSAID-induced gastric and duodenal ulcers and their complications.
From the U.S. FDA-approved label for Misoprostol. Full label: DailyMed.
Diclofenac sodium and misoprostol delayed-release tablets are indicated for treatment of the signs and symptoms of osteoarthritis or rheumatoid arthritis in adult patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications. For a list of factors that may increase the risk of NSAID-induced gastric and duodenal ulcers and their complications.
From the U.S. FDA-approved label for Misoprostol. Full label: DailyMed.
Use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals. Osteoarthritis: The recommended dosage for maximal GI protection is one tablet (containing 50 mg of diclofenac and 200 mcg of misoprostol) three times daily. Rheumatoid Arthritis: The recommended dosage for maximal GI protection is one tablet (containing 50 mg of diclofenac and 200 mcg of misoprostol) three or four times daily.
Directions from the U.S. FDA-approved label for Misoprostol — your doctor or pharmacist may advise differently.
Diclofenac sodium and misoprostol delayed-release tablets are contraindicated in the following patients: Pregnancy. Use of misoprostol, a component of diclofenac sodium and misoprostol delayed-release tablets, during pregnancy can result in maternal and fetal harm, including uterine rupture, abortion, premature birth, or birth defects In the setting of coronary artery bypass graft (CABG) surgery Active gastrointestinal bleeding History of asthma, urticaria, or other allergic-type reactions after taking aspirin or other NSAIDs.
Excerpt from the U.S. FDA-approved label for Misoprostol. Talk to a pharmacist or doctor before use.
Embryo-Fetal Toxicity with NSAIDs: Use of NSAIDs, including diclofenac in women at about 20 weeks gestation and later in pregnancy may cause oligohydramnios/fetal renal dysfunction and premature closure of the fetal ductus arteriosus. Hepatotoxicity: Inform patients of warning signs and symptoms of hepatotoxicity. Discontinue if abnormal liver tests persist or worsen or if clinical signs and symptoms of liver disease develop. Hypertension: Patients taking some antihypertensive medications may have impaired response to these therapies when taking NSAIDs. Monitor blood pressure.
Warnings and precautions excerpt from the U.S. FDA-approved label for Misoprostol — not a complete list. Talk to a pharmacist or doctor before use.
The following adverse reactions are discussed in greater detail in other sections of the labeling: Cardiovascular Thrombotic Events GI Bleeding, Ulceration and Perforation Hepatotoxicity Hypertension Heart Failure and Edema Renal Toxicity and Hyperkalemia Anaphylactic Reactions Serious Skin Reactions Hematologic Toxicity Most common adverse reactions (>2%) are: abdominal pain, diarrhea, dyspepsia, nausea, flatulence,…
Excerpt from the U.S. FDA-approved label for Misoprostol — not a complete list. Talk to a pharmacist or doctor about side effects.
8 brands · 5 makers in the NepalDoc catalog — see the full Misoprostol guide →
Store at 20° to 25°C (68° to 77°F).
Storage information from the U.S. FDA-approved label for Misoprostol.
What is Misoprost?
Misoprost 200mcg Tablet is a Misoprostol medicine made by Cipla Ltd. It comes as 200mcg Tablet.
What is the generic name of Misoprost?
The generic name of Misoprost is Misoprostol.
Which brands of Misoprostol are available in Nepal?
8 brands of Misoprostol are listed in the NepalDoc catalog, from 5 makers — including Isovent 200mcg Tablet, Misopil 200mcg Tablet, Misoprost 100mcg Tablet, Mistol 200mcg Tablet, Zitotec 100mcg Tablet, Zitotec 200mcg Tablet.
What are the side effects of Misoprostol?
The following adverse reactions are discussed in greater detail in other sections of the labeling: Cardiovascular Thrombotic Events GI Bleeding, Ulceration and Perforation Hepatotoxicity Hypertension Heart Failure and Edema Renal Toxicity and Hyperkalemia Anaphylactic Reactions Serious Skin Reactions Hematologic Toxicity Most common adverse reactions (>2%) are: abdominal pain, diarrhea, dyspepsia, nausea, flatulence,…
This page is information only and is not medical advice. Medicine details come from the sources listed above and may change — always confirm the medicine, strength and dose with a pharmacist or doctor before use. A catalog listing does not guarantee that a medicine is in stock at any pharmacy.
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