December 12, 2011 — Very-low-birth-weight newborns given ranitidine, a therapy for stress ulcers and gastroesophageal reflux disease (GERD), are about 6 times more likely to die than similar newborns ...
The U.S. Food and Drug Administration announced Wednesday it is requesting manufacturers remove all prescription and over-the-counter ranitidine drugs from the market immediately. This is the latest ...
More prescription-strength and hospital-used ranitidine, sold over the counter under the brand name Zantac, has been recalled for having too much of carcinogen NDMA. Though the run of recalls on the ...
If you go to your local pharmacy or convenience store, you won’t be able to find any Zantac or other products made out of ranitidine. At least, you shouldn’t. But it’s not because people are hoarding ...
A list of recalled versions of ranitidine, the heartburn/digestive medication called “Zantac” in name-brand form, now includes Publix’s over-the-counter store brand. Publix Maximum Strength Ranitidine ...
The U.S. Food and Drug Administration (FDA) is urging manufacturers of the heartburn drug ranitidine, commonly known as Zantac, to immediately remove the product from the market. The withdrawal ...
The U.S. Food and Drug Administration announced Wednesday it is requesting manufacturers remove all prescription and over-the-counter ranitidine drugs from the market immediately. This is the latest ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results