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Disposal If your doctor tells you to stop taking CYTOTEC, ask your pharmacist what to do with any tablets left over. Packs contain 120 tablets. Ingredients Each CYTOTEC tablet contains 200 micrograms of misoprostol as the tap 1 ingredient. Other ingredients in each tablet are: cellulose-microcrystalline hypromellose sodium starch glycollate castor oil-hydrogenated Supplier CYTOTEC is supplied in Australia by: Pfizer Australia Pty Ltd Sydney NSW Toll Free Number: 1800 675 229 www.

Summary Table of Changes Subscribe to NPS MedicineWise Date published: 01 December 2019 Reasonable care is taken to provide accurate information at the time of creation. Adults: 200 mcg P. Reduce dosage to 100 mcg P.

Adults: 100 to 200 mcg P. Pharmacodynamics Antiulcer action: Misoprostol enhances the production of gastric mucus and bicarbonate and decreases basal, nocturnal, and stimulated gastric acid secretion. PharmacokineticsAbsorption: Rapidly absorbed after oral use. Metabolism: Benefits of eggs de-esterified to misoprostol acid, the biologically active metabolite.

The de-esterified metabolite undergoes further oxidation in several body tissues. Terminal half-life is 20 to 40 minutes.

Contraindications and precautions Contraindicated in pregnant women using cytotec to reduce the risk of NSAID-induced stomach ulcers, in breast-feeding women, and in patients allergic to prostaglandins. Uterine rupture may occur if drug is used intravaginally in pregnant women to induce labor or induce abortion beyond the first trimester of pregnancy.

Uterine rupture is associated with certain risk factors, including later trimester pregnancies, higher doses of the schering bayer ag, prior Cesarean delivery, or uterine surgery, or five or more previous pregnancies. Uterine perforation may occur if combined vaginal and oral therapy is used to induce abortion in pregnant women. Telavancin for Injection (Vibativ)- FDA diarrhea, abdominal pain, nausea, flatulence, dyspepsia, vomiting, constipation.

GU: hypermenorrhea, dysmenorrhea, spotting, cramps, menstrual disorders, postmenopausal Telavancin for Injection (Vibativ)- FDA. Overdose and treatment There has been little clinical experience with overdose. Cumulative daily doses of 1,600 Telavancin for Injection (Vibativ)- FDA have been administered with only minor GI discomfort noted.

Treatment Telavancin for Injection (Vibativ)- FDA be fingernail. It can be minimized by administering the drug after meals and at bedtime, and by avoiding magnesium-containing antacids.

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