Difference between revisions of "Adverse drug event"
From Clinfowiki
(Created page with "'''An adverse event''' is any undesirable experience associated with the use of a medical product in a patient. The event is serious and should be reported to FDA when the patien...") |
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Required Intervention to Prevent Permanent Impairment or Damage (Devices) | Required Intervention to Prevent Permanent Impairment or Damage (Devices) | ||
Other Serious (Important Medical Events) | Other Serious (Important Medical Events) | ||
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| + | == Important interactions == | ||
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| + | [[Drug-drug interactions]] | ||
| + | [[Drug-allergy interactions]] | ||
| + | [[Drug-food interactions]] | ||
| + | [[Drug-laboratory interactions]] | ||
| + | [[Drug-tobacco interactions]] | ||
== References == | == References == | ||
# What is a Serious Adverse Event? FDA. [http://www.fda.gov/Safety/MedWatch/HowToReport/ucm053087.htm] | # What is a Serious Adverse Event? FDA. [http://www.fda.gov/Safety/MedWatch/HowToReport/ucm053087.htm] | ||
Revision as of 18:32, 17 November 2011
An adverse event is any undesirable experience associated with the use of a medical product in a patient. The event is serious and should be reported to FDA when the patient outcome is:
Death Life-threatening Congenital Anomaly/Birth Defect Required Intervention to Prevent Permanent Impairment or Damage (Devices) Other Serious (Important Medical Events)
Important interactions
Drug-drug interactions Drug-allergy interactions Drug-food interactions Drug-laboratory interactions Drug-tobacco interactions
References
- What is a Serious Adverse Event? FDA. [1]
