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  2. FDA Adverse Event Reporting System - Wikipedia

    en.wikipedia.org/wiki/FDA_Adverse_Event...

    Based on an evaluation of the potential safety concern, The FDA may take regulatory action(s) to improve product safety and protect the public health, such as updating a product's labeling information, restricting the use of the drug, communicating new safety information to the public, or, in rare cases, removing a product from the market.

  3. Pharmacovigilance - Wikipedia

    en.wikipedia.org/wiki/Pharmacovigilance

    Aggregate reporting, also known as periodic reporting, plays a key role in the safety assessment of drugs. Aggregate reporting involves the compilation of safety data for a drug over a prolonged period of time (months or years), as opposed to single-case reporting which, by definition, involves only individual AE reports.

  4. Research on Adverse Drug Events and Reports - Wikipedia

    en.wikipedia.org/wiki/Research_on_Adverse_Drug...

    RADAR is led by Dennis West. Though it was without funding for its first four years, RADAR has raised about $12 million through grants from the National Institutes of Health, the American Cancer Society and other such institutions. Its work has identified safety problems with 33 drugs. Adverse drug events are a serious health problem.

  5. US FDA widens probe of MDMA-based drug studies, WSJ reports - AOL

    www.aol.com/news/us-fda-widens-probe-mdma...

    The Food and Drug Administration investigators this week interviewed four people about the clinical trials sponsored by Lykos Therapeutics, the report said. Lykos did not immediately respond to a ...

  6. Adverse event - Wikipedia

    en.wikipedia.org/wiki/Adverse_event

    The FDA provides a database for reporting of adverse medical device events called the Manufacturer and User Facility Device Experience Database (MAUDE)[1]. The data consist of voluntary reports since June 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August 1996, and is open for public view.

  7. MedWatch - Wikipedia

    en.wikipedia.org/wiki/MedWatch

    The MedWatch system collects reports of adverse reactions and quality problems of drugs and medical devices but also for other FDA-regulated products (such as dietary supplements, cosmetics, medical foods, and infant formulas). As of the summer of 2011, the program had received more than 40,000 adverse event reports. [1]

  8. Thermo Fisher Scientific (TMO) Q3 2024 Earnings Call Transcript

    www.aol.com/thermo-fisher-scientific-tmo-q3...

    Image source: The Motley Fool. Thermo Fisher Scientific (NYSE: TMO) Q3 2024 Earnings Call Oct 23, 2024, 8:30 a.m. ET. Contents: Prepared Remarks. Questions and Answers. Call Participants

  9. Vaccine Adverse Event Reporting System - Wikipedia

    en.wikipedia.org/wiki/Vaccine_Adverse_Event...

    Due to the program's open and accessible design and its allowance of unverified reports, incomplete VAERS data is often used in false claims regarding vaccine safety. [ 14 ] [ 15 ] [ 16 ] The Centers for Disease Control and Prevention (CDC) has warned that raw data from VAERS is not enough to determine whether a vaccine can cause a particular ...