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Naproxen/diphenhydramine (trade name Aleve PM) is a formulation of naproxen with diphenhydramine marketed by Bayer Healthcare. [1] It is made as an over-the-counter drug . The intended use of the drug is relieve pain specifically when going to sleep.
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
This year’s recall involves over 300 products and 23 states. Earlier in 2022, a rodent infestation at a Family Dollar distribution facility caused a recall of over-the-counter drugs, dietary ...
Pharmacists and parents are struggling to find children’s pain- and fever- reducing medications like Tylenol, Advil and Motrin. Here are recommended alternatives. Children's medication shortages ...
Naproxen's medical uses are related to its mechanism of action as an anti-inflammatory compound. [11] Naproxen is used to treat a variety of inflammatory conditions and symptoms that are due to excessive inflammation, such as pain and fever (naproxen has fever-reducing, or antipyretic, properties in addition to its anti-inflammatory activity). [11]
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According to the U.S. Food and Drug Administration’s (FDA) recall alert, 39 people have been infected with Shiga toxin-producing E. coli. in 18 states, including Michigan.