Difference between revisions of "Adverse drug event"
From Clinfowiki
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== Important interactions == | == Important interactions == | ||
− | [[Drug-drug interactions]] | + | * [[Drug-drug interactions]] |
− | [[Drug-allergy interactions]] | + | * [[Drug-allergy interactions]] |
− | [[Drug-food interactions]] | + | * [[Drug-food interactions]] |
− | [[Drug-laboratory interactions]] | + | * [[Drug-laboratory interactions]] |
− | [[Drug-tobacco 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 18:33, 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]