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  2. Serious adverse event - Wikipedia

    en.wikipedia.org/wiki/Serious_adverse_event

    Serious adverse reactions are serious adverse events judged to be related to drug therapy. A SUSAR (suspected unexpected serious adverse reaction) should be reported to a drug regulatory authority under an investigational license by using the CIOMS form (or in some countries an equivalent form).

  3. The James Cancer Hospital - Wikipedia

    en.wikipedia.org/wiki/The_James_Cancer_Hospital

    The ground breaking for the hospital was July 10, 1984. It was completed January 16, 1990 but a water main break delayed the opening until July 9, 1990, when the first patient was admitted.The hospital treats cancer, and conducts research in the Solove Research Institute. The James receives donations through the Pelotonia biking event.

  4. Adverse event - Wikipedia

    en.wikipedia.org/wiki/Adverse_event

    Adverse events categorized as "serious" (results in death, illness requiring hospitalization, events deemed life-threatening, results in persistent or significant incapacity, a congenital anomaly or medically important condition) must be reported to the regulatory authorities immediately, whereas non-serious adverse events are merely documented ...

  5. Electroconvulsive therapy - Wikipedia

    en.wikipedia.org/wiki/Electroconvulsive_therapy

    A 2019 systematic review and meta-analysis of 82 studies found that the rate of major adverse cardiac events with ECT was 1 in 39 patients or about 1 in 200 to 500 procedures. [80] [81] The risk of death with ECT however is low. [82] [80] If death does occur, cardiovascular complications are considered as causal in about 30% of individuals. [80]

  6. Patient safety - Wikipedia

    en.wikipedia.org/wiki/Patient_safety

    After an adverse event occurs, each country has its own way of dealing with the incident. In Canada, a quality improvement review is primarily used. A quality improvement review is an evaluation that is completed after an adverse event occurs with the intention to both fix the problem as well as prevent it from happening again. [41]

  7. 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).