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  2. American Health Care Academy - Wikipedia

    en.wikipedia.org/wiki/American_Health_Care_Academy

    The idea for AHCA came to him in 2009 after a choking incident involving an infant, which highlighted the need for accessible CPR training. AHCA was launched as an online training platform in Texas [1] [3] and expanded to Vietnam in July 2019, the Philippines in May 2018, and later to Mexico, Latvia, India, and Pakistan. [4]

  3. Serious adverse event - Wikipedia

    en.wikipedia.org/wiki/Serious_adverse_event

    In drug development, serious adverse event (SAE) is defined as any untoward medical occurrence during a human drug trial that at any dose Results in death; Is life-threatening; Requires inpatient hospitalization or causes prolongation of existing hospitalization; Results in persistent or significant disability/incapacity

  4. 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.

  5. Common Terminology Criteria for Adverse Events - Wikipedia

    en.wikipedia.org/wiki/Common_Terminology...

    The Common Terminology Criteria for Adverse Events (CTCAE), [1] formerly called the Common Toxicity Criteria (CTC or NCI-CTC), are a set of criteria for the standardized classification of adverse events of drugs and treatment used in cancer therapy. The CTCAE system is a product of the US National Cancer Institute (NCI).

  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. FDA Adverse Event Reporting System - Wikipedia

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

    The FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) postmarketing safety surveillance program for all approved drug and therapeutic biologic products.

  8. American Health Care Association - Wikipedia

    en.wikipedia.org/wiki/American_Health_Care...

    The American Health Care Association (AHCA) is a non-profit federation of affiliated state health organizations that represents more than 14,000 non-profit and for-profit nursing homes, assisted living communities, [1] and facilities for individuals with disabilities. Clifton J. Porter, II became CEO on 14 October 2024.

  9. Incident report - Wikipedia

    en.wikipedia.org/wiki/Incident_report

    Generally, according to health care guidelines, the report must be filled out as soon as possible following the incident (but after the situation has been stabilized). This way, the details written in the report are as accurate as possible. [2] Most incident reports that are written involve accidents with patients, such as patient falls. But ...