Difference between revisions of "Adverse drug event"

From Clinfowiki
Jump to: navigation, search
 
(4 intermediate revisions by one user not shown)
Line 1: Line 1:
'''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:
+
An '''adverse event (ADE)''' is any undesirable experience associated with the use of a medical product in a patient. The event is serious and should be reported to [[U.S. Food and Drug Administration (FDA)]] when the patient outcome is:
  
 
* Death
 
* Death
Line 6: Line 6:
 
* 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)
 +
 +
== Clinical Decision Support ==
 +
 +
Rules for ADE are often used in [[CDS|clinical decision support systems]].
  
 
== Important interactions ==
 
== Important interactions ==
Line 14: Line 18:
 
* [[Drug-laboratory interaction]]
 
* [[Drug-laboratory interaction]]
 
* [[Drug-tobacco interaction]]
 
* [[Drug-tobacco interaction]]
 +
 +
== Reviews ==
 +
 +
* [[Risk factors for adverse drug events]]
 +
* [[Criteria for assessing high-priority drug-drug interactions for clinical decision support in electronic health records]]
 +
* [[Can Utilizing a Computer Provider Order Entry (CPOE) System Prevent Hospital Medical Errors and Adverse Drug Events?]]
  
 
== 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]

Latest revision as of 22:02, 4 November 2015

An adverse event (ADE) is any undesirable experience associated with the use of a medical product in a patient. The event is serious and should be reported to U.S. Food and Drug Administration (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)

Clinical Decision Support

Rules for ADE are often used in clinical decision support systems.

Important interactions

Reviews

References

  1. What is a Serious Adverse Event? FDA. [1]