ranitidine
Zantac
On April 1, 2020, the FDA requested the removal of all ranitidine products from the market (over-the-counter and prescription) immediately due to a contaminant known as NDMA, a probable human carcinogen.
75mg, 150mg, and 300mg tablets; 150mg and 300mg capsules; 15mg/mL syrup, 25mg/mL injectable solution
Histamine-2 blocker
Stomach ulcers, intestinal ulcers, stress-related gastritis, drug-induced gastritis, esophagitis, and esophageal reflux
Ranitidine decreases the amount of acid that is produced in the stomach by inhibiting the histamine-2 receptor. Decreasing the amount of acid in the stomach produces a more favorable environment to rest and heal.
Vomiting, diarrhea, irregular heartbeat, rapid breathing, muscle tremors, lack of coordination, light-headedness, fainting
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