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  2. Atorvastatin - Wikipedia

    en.wikipedia.org/wiki/Atorvastatin

    Atorvastatin is a statin medication used to prevent cardiovascular ... The FDA received no reports of ... Ranbaxy also issued recalls of bottles of 10-milligram ...

  3. List of withdrawn drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_withdrawn_drugs

    Cardiac valvular disease, pulmonary hypertension, cardiac fibrosis; [3] [23] re-approved in June 2020 for the treatment of seizures associated with Dravet syndrome, under FDA orphan drug rules. Fenoterol: 1990 New Zealand Asthma mortality. [3] Feprazone: 1984 Germany, UK Cutaneous reaction, multiorgan toxicity. [3] Fipexide: 1991 France ...

  4. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    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]

  5. A drug made by a Florida company has been recalled for a ...

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    Lighter Side. Medicare. new

  6. 2 medications from 1 manufacturer recalled for a failure that ...

    www.aol.com/2-medications-1-manufacturer...

    The batch numbers are in a PDF attached to the FDA recall notice posting. The label for Glenmark Pharmaceuticals Potassium Chloride Extended Release Capsules 100-count bottles, which were recalled ...

  7. A drug made by a Florida company has been recalled for a ...

    www.aol.com/drug-made-florida-company-recalled...

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  8. Cerivastatin - Wikipedia

    en.wikipedia.org/wiki/Cerivastatin

    Cerivastatin (INN, [1] brand names: Baycol, Lipobay) is a synthetic member of the class of statins used to lower cholesterol and prevent cardiovascular disease.It was marketed by the pharmaceutical company Bayer A.G. in the late 1990s, competing with Pfizer's highly successful atorvastatin (Lipitor).

  9. More than 233,000 bottles of duloxetine capsules sold by Rising Pharmaceuticals were voluntarily recalled on Nov. 19, and the U.S. Food and Drug Administration assigned the recall as a class II ...