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  2. FDA warning letter - Wikipedia

    en.wikipedia.org/wiki/FDA_Warning_Letter

    Warning Letters should only be issued for violations of regulatory significance, i.e., those that may actually lead to an enforcement action if the documented violations are not promptly and adequately corrected. A Warning Letter is one of the Agency's principal means of achieving prompt voluntary compliance with the Act. [1]

  3. Category:Standardised user warning templates - Wikipedia

    en.wikipedia.org/wiki/Category:Standardised_user...

    [[Category:Standardised user warning templates]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Standardised user warning templates]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.

  4. Boxed warning - Wikipedia

    en.wikipedia.org/wiki/Boxed_warning

    In the United States, a boxed warning (sometimes "black box warning", colloquially) is a type of warning that appears near the beginning of the package insert for certain prescription drugs, so called because the U.S. Food and Drug Administration specifies that it is formatted with a 'box' or border around the text [1] to emphasize its ...

  5. Template:Warn - Wikipedia

    en.wikipedia.org/wiki/Template:Warn

    Beyond those listed above, there are also higher level warnings for continued unconstructive editing (see the template documentation for details); if previous warnings have been given under that title, add the next level warning beneath the others, within that section. Individual cases must be dealt with as seems appropriate.

  6. Form FDA 483 - Wikipedia

    en.wikipedia.org/wiki/Form_FDA_483

    The header identifies the FDA district office that performed the inspection, the date(s) of inspection, name and address of the facility that was inspected, the name and title of the individual to whom the 483 is issued to (usually the most responsible individual physically present in the facility), a brief description of the type of facility, and the facility's FEI (FDA Establishment ...

  7. US FDA sends warning letter to Cardinal Health for marketing ...

    www.aol.com/news/us-fda-sends-warning-cardinal...

    US FDA sends warning letter to Cardinal Health for marketing unapproved devices. April 25, 2024 at 12:13 PM (Reuters) -The U.S. health regulator has sent a warning letter to Cardinal Health after ...

  8. Metronidazole - Wikipedia

    en.wikipedia.org/wiki/Metronidazole

    Metronidazole, sold under the brand name Flagyl among others, is an antibiotic and antiprotozoal medication. [10] It is used either alone or with other antibiotics to treat pelvic inflammatory disease, endocarditis, and bacterial vaginosis. [10] It is effective for dracunculiasis, giardiasis, trichomoniasis, and amebiasis. [10]

  9. Benzodiazepine withdrawal syndrome - Wikipedia

    en.wikipedia.org/wiki/Benzodiazepine_withdrawal...

    Benzodiazepine withdrawal syndrome (BZD withdrawal) is the cluster of signs and symptoms that may emerge when a person who has been taking benzodiazepines as prescribed develops a physical dependence on them and then reduces the dose or stops taking them without a safe taper schedule.