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  2. Yellow Card Scheme - Wikipedia

    en.wikipedia.org/wiki/Yellow_Card_Scheme

    The types of adverse reactions that should be reported are: Those that have caused death or a serious illness; Any adverse reaction, however minor, if associated with a new medicine or one that is under continued monitoring (highlighted in the British National Formulary with a black triangle)

  3. Adverse drug reaction - Wikipedia

    en.wikipedia.org/wiki/Adverse_drug_reaction

    Type A: augmented pharmacological effects, which are dose-dependent and predictable [5]; Type A reactions, which constitute approximately 80% of adverse drug reactions, are usually a consequence of the drug's primary pharmacological effect (e.g., bleeding when using the anticoagulant warfarin) or a low therapeutic index of the drug (e.g., nausea from digoxin), and they are therefore predictable.

  4. Template:Infobox drug/testcases-warning - Wikipedia

    en.wikipedia.org/wiki/Template:Infobox_drug/test...

    This is the template test cases page for the sandbox of Template:Infobox drug to update the examples. If there are many examples of a complicated template, later ones may break due to limits in MediaWiki; see the HTML comment "NewPP limit report" in the rendered page. You can also use Special:ExpandTemplates to examine the results of template uses. You can test how this page looks in the ...

  5. Pharmacovigilance - Wikipedia

    en.wikipedia.org/wiki/Pharmacovigilance

    A risk management plan is a documented plan that describes the risks (adverse drug reactions and potential adverse reactions) associated with the use of a drug and how they are being handled (warning on drug label or on packet inserts of possible side effects which if observed should cause the patient to inform/see his physician and/or ...

  6. Adverse effect - Wikipedia

    en.wikipedia.org/wiki/Adverse_effect

    Adverse reaction reporting is an important component of New Zealand's pharmacovigilance activities. The Centre for Adverse Reactions Monitoring (CARM) in Dunedin is New Zealand's national monitoring centre for adverse reactions. It collects and evaluates spontaneous reports of adverse reactions to medicines, vaccines, herbal products and ...

  7. Template:Drug reactions - Wikipedia

    en.wikipedia.org/wiki/Template:Drug_reactions

    Template documentation This template's initial visibility currently defaults to autocollapse , meaning that if there is another collapsible item on the page (a navbox, sidebar , or table with the collapsible attribute ), it is hidden apart from its title bar; if not, it is fully visible.

  8. WHOART - Wikipedia

    en.wikipedia.org/wiki/WHOART

    The WHO Adverse Reactions Terminology (WHOART) was a dictionary meant to serve as a basis for rational coding of adverse reaction terms. The system was maintained by the Uppsala Monitoring Centre (UMC), the World Health Organization Collaborating Centre for International Drug Monitoring. The system is no longer actively maintained since 2015.

  9. FDA Adverse Event Reporting System - Wikipedia

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

    Further, the FDA does not receive all adverse event reports that occur with a product. Many factors can influence whether or not an event will be reported, such as the time a product has been marketed and publicity about an event. Therefore, FAERS cannot be used to calculate the incidence of an adverse event in the U.S. population.

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