Ranitidine ip 150 mg

Ranitidine belongs to the class of medications called H2-antagonists. It works by reducing the ranitidine ip 150 mg 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, ranitidine ip 150 mg. It is used to treat stomach and duodenal intestinal ulcers, and prevent them from recurring.

If you are a consumer or patient please visit this version. Chemically it is N[2-[[[5-[ dimethylamino methyl]furanyl]methyl]thio]ethyl]-N'-methylnitro-1,1-ethenediamine, HCl. It has the following structure:. Ranitidine HCl is a white to pale yellow, granular substance that is soluble in water. It has a slightly bitter taste and sulfur like odor. Ranitidine Tablets are a competitive, reversible inhibitor of the action of histamine at the histamine H 2 -receptors, including receptors on the gastric cells.

Ranitidine ip 150 mg

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 In April , ranitidine was withdrawn from the United States market and suspended in the European Union and Australia due to these concerns.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 Ranitidine was discovered in England in , and came into commercial use in It has been withdrawn at regulator request from most markets, including the United States; [12] it has been discontinued globally, according to the NHS.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. Rare reports have been made of ranitidine causing malaise , dizziness , somnolence , insomnia , and vertigo. In severely ill, elderly patients, cases of reversible mental confusion, agitation, depression, and hallucinations have been reported. Arrhythmias such as tachycardia , bradycardia , atrioventricular block , and premature ventricular beats have also been reported. All drugs in the H 2 receptor blocker class of medicines have the potential to cause vitamin B 12 deficiency, secondary to a reduction in food-bound vitamin B 12 absorption.

Unreviewed reports. Arrhythmias such as tachycardiabradycardiaatrioventricular blockand premature ventricular beats have also been reported.

Ranitidine MG Tablet is prescribed as the short-term treatment of active duodenal ulcers and benign gastric ulcers. This medicine is also prescribed for long-term prophylaxis of duodenal ulcer and gastric hypersecretory states, recurrent postoperative ulcer, prevention of acid-aspiration pneumonitis during surgery, and prevention of stress-induced ulcers; causes fewer interactions than cimetidine. This medicine belongs to a drug group known as histamine H2 receptor blocker. Ranitidine MG Tablet works by reducing the amount of acid produced in the stomach, effectively treating gastroesophageal reflux disease GERD , Zollinger-Ellison syndrome and upper GI bleeding ulcers. Patients need to be aware that intake of this medicine can increase the chances of succumbing to pneumonia.

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 ip 150 mg

If you are a consumer or patient please visit this version. Allergy alert: Do not use if you are allergic to ranitidine or any other acid reducers. If pregnant or breastfeeding , ask a health professional before use.

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Instead, the best way to dispose of your medication is through a medicine take-back program. Smaller doses have been shown to be equally effective in inhibiting gastric acid secretion in US studies, and several foreign trials have shown that mg twice daily is as effective as the mg dose. Medical Dialogues. If you become pregnant while taking this medication, contact your doctor immediately. Archived from the original on 4 August Of the total number of subjects enrolled in US and foreign controlled clinical trials of oral formulations of Ranitidine Tablets, for which there were subgroup analyses, 4, were 65 and over, while were 75 and over. Ans : This medication starts working as fast as 15 minutes from when it is given. Symptomatic relief of heartburn commonly occurs within 24 hours of therapy initiation with Ranitidine Tablets USP, mg 4 times daily. Are there any overdose instructions? Delavirdine: Delavirdine absorption may be impaired based on known interactions with other agents that increase gastric pH. Do not chew or let the effervescent tablet dissolve after you place it in your mouth. Archived from the original on 21 January

Last Updated: November 7, References.

Pathological Hypersecretory Conditions such as Zollinger - Ellison syndrome : The current recommended adult oral dosage is mg twice daily. Kidney function: Kidney disease or reduced kidney function may cause this medication to build up in the body, causing side effects. Official websites use. Take exactly as directed at meals and bedtime ; do not increase dose - may take several days before you notice relief. No information regarding dose adjustment is available in hepatic patients. The following have been reported as events in clinical trials or in the routine management of patients treated with Ranitidine Tablets. Rare reports have been made of ranitidine causing malaise , dizziness , somnolence , insomnia , and vertigo. Table 3. In the elderly population, the plasma half-life of ranitidine is prolonged to 3—4 hours secondary to decreased kidney function causing decreased clearance. Wikimedia Commons. Many things can affect the dose of medication that a person needs, such as body weight, other medical conditions, and other medications.