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  2. October 24, 2024 at 1:03 PM. ... is at the center of the FDA's recall. ... Nitrosamines below this level are acceptable in drugs,” the FDA says on its website. “If drugs contain levels of ...

  3. FDA recalls more than 7,000 bottles of antidepressant over a ...

    www.aol.com/fda-recalls-more-7-000-154029555.html

    The Food and Drug Administration announced a Class II recall for more than 7,000 bottles of an antidepressant due to a chemical.. The recall was initiated earlier this month on Oct. 10. Duloxetine ...

  4. Why Are There So Many Recalls Right Now? We Asked the FDA - AOL

    www.aol.com/why-many-recalls-now-asked-211253431...

    I talked to the U.S. Food & Drug Administration’s (FDA) spokesperson Janell Goodwin. ... She even provided this chart to show the comparison between the amount of recalls in 2024 versus the ...

  5. 2024 United States drug shortages - Wikipedia

    en.wikipedia.org/wiki/2024_United_States_drug...

    The American Society of Health-System Pharmacists (ASHP) reported that 323 "active medication shortages" were reported in January–March 2024. As a result of drug scarcity, many healthcare systems were forced to either ration out essential drugs, triage patients based on the severity of their condition and their need for the drug, or both.

  6. List of withdrawn drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_withdrawn_drugs

    Diversion, abuse, and a relatively high rate of overdose deaths in comparison to other drugs of its group. This drug continues to be available in most of the world including the US, but under strict controls. Terfenadine (Seldane, Triludan) 1997–1998 France, South Africa, Oman, others, US Prolonged QT interval; ventricular tachycardia [2] [3]

  7. 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]

  8. The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine due to the possible presence of a carcinogen. Duloxetine belongs to a ...

  9. U.S. Consumer Product Safety Commission - Wikipedia

    en.wikipedia.org/wiki/U.S._Consumer_Product...

    Old logo (1972-2018) The United States Consumer Product Safety Commission (USCPSC, CPSC, or commission) is an independent agency of the United States government.The CPSC seeks to promote the safety of consumer products by addressing "unreasonable risks" of injury (through coordinating recalls, evaluating products that are the subject of consumer complaints or industry reports, etc ...