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There are 27 eye drops that might cause you to go blind, FDA says. Here are the products consumers should avoid.
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.
One brand says it knows of blurred vision and vision loss from users. These recalls follow FDA warnings about eye drops sold under brands such as CVS Health, Target’s Up & Up and Rite Aid’s ...
Metoprolol, sold under the brand name Lopressor among others, is a medication used to treat angina, high blood pressure and a number of conditions involving an abnormally fast heart rate. [4] It is also used to prevent further heart problems after myocardial infarction and to prevent headaches in those with migraines . [ 4 ]
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 ...
Not all Prograf and Astagraf XL on the market have been recalled. Recalled Prograf is 0.5 mg strength, in 100-count bottles from lot No. 0E3353D. The recalled Astagraf comes in 30-count bottles of ...
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