Ranitidine tablets ip 150 mg uses

If you are a consumer or patient please visit this version. Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers. In case of overdose, get medical help or contact a Poison Control Center right away.

Ranitidine , sold under the brand name Zantac among others, is a medication used to decrease stomach acid production. In September , the probable carcinogen N -nitrosodimethylamine NDMA was discovered in ranitidine products from a number of manufacturers, resulting in recalls. In , these concerns were confirmed in a nationwide [ which? Common side effects include headaches and pain or burning if given by injection. Ranitidine was discovered in England in , and came into commercial use in It has been withdrawn at regulator request from most markets, including the United States; [12] it has been discontinued globally, according to the NHS. Ranitidine has been discontinued globally, according to the NHS , [30] and is contraindicated due to excess cancer risk and the ready availability of H2 antagonist and PPI alternatives.

Ranitidine tablets ip 150 mg uses

Author Details. Radhika Dua. Shilpa Garcha. We provide you with authentic, trustworthy and relevant information Want to know more. Have issue with the content? Report Problem. Rantidine mg Tablet. Ranitidine mg. Click here to view all substitutes. Product introduction Rantidine mg Tablet is a medicine that reduces the amount of acid your stomach makes. It is used to treat and prevent heartburn, indigestion, and other symptoms caused by too much acid in the stomach. It is also used to treat and prevent stomach ulcers, reflux disease, and some rarer conditions. Rantidine mg Tablet is also commonly prescribed to prevent stomach ulcers and heartburn seen with the use of painkillers.

Use of these two medications together should be avoided. Rantidine mg Tablet is generally considered safe to use during pregnancy.

Chemically it is N[2-[[[5-[ dimethylamino methyl]furanyl]methyl]thio]ethyl]-N'-methylnitro-1,1-ethenediamine, HCl. It has the following structure:. HCl, representing molecular weight of Ranitidine HCl is white to pale yellow, crystalline, practically odorless powder, sensitive to light and moisture. Ranitidine Tablets is a competitive, reversible inhibitor of the action of histamine at the histamine H 2 -receptors, including receptors on the gastric cells. Ranitidine Tablets is not an anticholinergic agent.

Author Details. Radhika Dua. Shilpa Garcha. We provide you with authentic, trustworthy and relevant information Want to know more. Have issue with the content?

Ranitidine tablets ip 150 mg uses

Official websites use. Share sensitive information only on official, secure websites. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine NDMA in ranitidine medications commonly known by the brand name Zantac. NDMA is a probable human carcinogen a substance that could cause cancer. FDA has determined that the impurity in some ranitidine products increases over time and when stored at higher than room temperatures may result in consumer exposure to unacceptable levels of this impurity. As a result of this immediate market withdrawal request, ranitidine products will not be available for new or existing prescriptions or OTC use in the U. Prescription ranitidine is approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease. Ranitidine is used to treat ulcers; gastroesophageal reflux disease GERD , a condition in which backward flow of acid from the stomach causes heartburn and injury of the food pipe esophagus ; and conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome.

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GERD or acid reflux is caused by the regurgitation of acidic liquid stomach contents back up into Archived from the original on 27 December Also tell your doctor what other medicines you are taking as some may affect, or be affected by, this medicine. Take one This medication is meant for oral consumption and should be swallowed immediately. Aanchal Maheshwari. Do not take over-the-counter Rantidine mg Tablet for longer than 2 weeks unless advised by your doctor. Is it safe to drive while on this medicine? It can be taken once daily before bedtime or twice daily in the morning and before bedtime, as recommended. Additional indirect effects of ranitidine are decreased pepsin secretion and increased nitrate-reducing bacterial flora. Symptomatic relief of heartburn commonly occurs within 24 hours of therapy initiation with Ranitidine Tablets USP, mg 4 times daily. The NDMA was generated by the added heat, but the higher temperatures are recommended for using a gas chromatography—mass spectrometry method to test for NDMA in valsartan and angiotensin II receptor blockers. August How should this medicine be used? As with other H 2 -antagonists, the factors responsible for the significant reduction in the prevalence of duodenal ulcers include prevention of recurrence of ulcers, more rapid healing of ulcers that may occur during maintenance therapy, or both.

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Archived from the original on 26 September No placebo — controlled comparative studies have been carried out for periods longer than 1 year. GERD: The current recommended adult oral dosage is mg twice daily. This damaged the stomach and allows an ulcer to form. It is suggested not to take Ranitidine MG Tablet with alcohol, as it is unsafe to take it concomitantly. You should take it for the duration advised by your doctor. Retrieved 30 March Table 2. Follow the directions on your prescription or the package label carefully, and ask your doctor or pharmacist to explain any part you do not understand. There is insufficient information about the pharmacokinetics of Ranitidine Tablets in neonatal patients less than 1 month of age to make dosing recommendations. Radhika Dua. Maintenance therapy in duodenal ulcer: Ranitidine has been found to be effective as maintenance therapy for patients following healing of acute duodenal ulcers. This may be a sign of a more serious condition. Increased toxicity of cyclosporine increased serum creatinine , gentamicin neuromuscular blockade , glipizide, glyburide, midazolam increased concentrations , metoprolol, pentoxifylline, phenytoin, quinidine.