Difference between revisions of "Adverse drug event"
From Clinfowiki
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== Important interactions == | == Important interactions == | ||
| − | * [[Drug-drug | + | * [[Drug-drug interaction]] |
| − | * [[Drug-allergy | + | * [[Drug-allergy interaction]] |
| − | * [[Drug-food | + | * [[Drug-food interaction]] |
| − | * [[Drug-laboratory | + | * [[Drug-laboratory interaction]] |
| − | * [[Drug-tobacco | + | * [[Drug-tobacco interaction]] |
== 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 18:39, 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 interaction
- Drug-allergy interaction
- Drug-food interaction
- Drug-laboratory interaction
- Drug-tobacco interaction
References
- What is a Serious Adverse Event? FDA. [1]
