Ranitidine ip 150 mg

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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.

Ranitidine ip 150 mg

Ranitidine belongs to the class of medications called H2-antagonists. It works by reducing the amount of acid secreted by the stomach in order to reduce ulcer and heartburn pain or to assist in healing of ulcers. Ranitidine is used to treat and prevent stomach ulcers caused by non-steroidal anti-inflammatory drugs NSAIDs ; to prevent bleeding caused by stress ulcers for very ill people; to prevent a second episode of bleeding in the digestive tract caused by bleeding ulcers; and to prevent inhalation of stomach acid during surgery, for people who are considered at risk of this complication. It is used to treat stomach and duodenal intestinal ulcers, and prevent them from recurring. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here. As well, some forms of this medication may not be used for all of the conditions discussed here. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor. Do not give this medication to anyone else, even if they have the same symptoms as you do.

Follow the directions on your prescription or the package label carefully, ranitidine ip 150 mg, and ask your doctor or pharmacist to explain any part you do not understand. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

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 April , ranitidine was withdrawn from the United States market and suspended in the European Union and Australia due to these concerns. 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

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. Keep the carton. It contains important information. DailyMed will deliver notification of updates and additions to Drug Label information currently shown on this site through its RSS feed. DailyMed will deliver this notification to your desktop, Web browser, or e-mail depending on the RSS Reader you select to use. Due to inconsistencies between the drug labels on DailyMed and the pill images provided by RxImage , we no longer display the RxImage pill images associated with drug labels. We anticipate reposting the images once we are able identify and filter out images that do not match the information provided in the drug labels.

Ranitidine ip 150 mg

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In children, the use of gastric acid inhibitors has been associated with an increased risk for development of acute gastroenteritis and community-acquired pneumonia. Ranitidine Tablets is a competitive, reversible inhibitor of the action of histamine at the histamine H 2 -receptors, including receptors on the gastric cells. High doses of ranitidine e. Very effective treatment is available Drug-induced thrombocytopenia usually takes weeks or months to appear, but may appear within 12 hours of drug intake in a sensitised individual. Elderly patients are more likely to have decreased renal function, therefore caution should be exercised in dose selection, and it may be useful to monitor renal function. Archived from the original on 24 October In normal volunteers, SGPT values were increased to atleast twice the pretreatment levels in 6 of 12 subjects receiving mg intravenously 4 times daily for 7 days, and in 4 of 24 subjects receiving 50 mg intravenously 4 times daily for 5 days. Nursing Mothers Ranitidine is secreted in human milk. American Journal of Clinical Medicine. Porphyria: Ranitidine may cause attacks of a condition called acute porphyria a disorder that affects the production of heme in the body. In September , the U. February

Last Updated: November 7, References.

Retrieved 29 September Integumentary: Rash, including rare cases of erythema multiforme. Placebo-controlled trials have been carried out for 48 weeks. How does this medication work? Kidney function: Kidney disease or reduced kidney function may cause this medication to build up in the body, causing side effects. Rosemont Pharmaceuticals Limited is recalling unexpired stock from pharmacies as a precautionary measure due to possible contamination with an impurity. CVS Health. In September , the probable carcinogen N -nitrosodimethylamine NDMA was discovered in ranitidine products from a number of manufacturers, resulting in recalls. Atazanavir: Atazanavir absorption may be impaired based on known interactions with other agents that increase gastric pH. Do not stop the usage of any medication without consulting your doctor. In April , the FDA requested a manufacturer's market withdrawal of ranitidine, [19] [] meaning that ranitidine products would not be available for prescription or over-the-counter sale in the U.