Ranitidine
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Ranitidine

Description
Ranitidine is a histamin H2 receptor antagonist. It inhibits basal and stimulated secretion of gastric acid. Ranitidine is rapidly absorbed after oral administration. Food or antacid does not interfere its absorption.

INDICATIONS
Ranitidine is indicated for the treatment of duodenal ulcer, benign gastric ulcer, postoperative ulcer, reflux esophagitis, zollinger-ellison syndrome and in other conditions where reduction of gastric acidity is beneficial.

CLINICAL PHARMACOLOGY
Renitidine is potent histamin HL receptor antagonist and inhibits gastric acid secretion elicited by histamine. Renitidine also inhibits acid secretion elicited by gastrin and, to a lesser extent, by muscarinic agonists. Renitidine inhibits basal and nocturnal acid secretion and that simulated by food, fundic distention, and various drugs. It reduces both the volume and acid concentration of gastric juice. the out put of pepsin and secretion of intrinsic factor are also reduced.
Ranitidine is readily absorbed from the gastrointestinal tract with peak concentration in plasma occurring about 2 to 3 hours after oral administration. The bioavailability of ranitidine is about 50% due to first-pass metabolism. The elimination half-life from plasma is around 2 to 3 hours and ranitidine is weakly bound to plasma protein (about 15%). A small proportion of ranitidine is metabolized in the liver and is excreted unchanged in the urine. ranitidine crosses the placental barrier and is excreted into breast milk.

Dosage And Administration
Duodenal and Gastric ulcer : The usual dosage is 150 mg twice daily taken in the morning and evening or 300 mg as a single dose at night for 4 to 8 weeks.
Reflux esophagitis : 150 mg twice daily or 300mg at bed time for up to 8 weeks.
Zollinger-Ellison syndrome : 150 mg 3 times daily, if necessary increased up to 6g daily in divided doses. Dosages should be continued as long as clinically indicated.
Episodic Dyspepsia : 150 mg twice daily or 300 mg at bed time for up to 6 weeks.
Maintenance therapy : 150 mg at night for preventing ulcer recurrences.
Side Effects
Ranitidine is well toleratd and side effects are usually uncommon. Altered bowel habit, dizziness, rash, tiredness, reversible confessional states, headache, ecreased blood counts, muscle or joint pain have rarely been reported.
Precautions
Ranitidine should be given in reduced dosage to patients with impaired renal and hepatic function.
Pregnancy
Ranitidine crosses the placenta. But there is no evidence of impaired fertility or harm to the fetus due to Ranitidine. Like other drugs, Ranitidine should only be used during pregnancy if considered essential.
Nursing Mothers
Ranitidine is excreted in human breast milk. Caution should be exercised when the drug is administered to a nursing mother.
Pharmaceutical Precautionss
Store in a cool and dry place. Protect from light.

Name of Product
Pharmaceuticals
Acin Bio-Pharma
Denitine Doctor's Chemical Works
Editin-R Edruk
Gepin General Pharma
Hi-Tac Hudson
Inseac Inseac
Lumeran Ariastopharma
Neoceptin-R Beximco
Neotac Square pharma
Neotin Nipa
Norma-H Renata
Peptil-H Eskayef
Ranitidin Acme
Rani-150 Alco Pharma
Ranison

Jayson Pharma

Ranitid Opsonin Chemical
Ranitidin-R Remedy Pharma
Ranix Chemist Lab
Reetac-R Navana
Renicon Medicon
Ulcar Drug International
Ultradin-150 Globe
Xantid/Xantid-HS ACI
Zactin Aventis Pharma
Zantac GlaxoSmithKline
Zodin Somatec
Zorep Amico
     
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Revised & Updated on 19-07-06.
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