Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Charleston Antidepressant Drug Interactions Surveillance Program (CADISP).

C L DeVane1, J S Markowitz, H L Liston

  • 1Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, 67 President Street, Charleston, SC 29425-0742, USA. devaneL@musc.edu

Psychopharmacology Bulletin
|October 26, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Development of a Longitudinal National Football League Injury and Injury Impacts (L-NFL-III) Database.

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research·2016
Same author

Clopidogrel bioactivation and risk of bleeding in patients cotreated with angiotensin-converting enzyme inhibitors after myocardial infarction: a proof-of-concept study.

Clinical pharmacology and therapeutics·2014
Same author

The psychostimulant d-threo-(R,R)-methylphenidate binds as an agonist to the 5HT(1A) receptor.

Die Pharmazie·2009
Same author

Influence of ethanol and gender on methylphenidate pharmacokinetics and pharmacodynamics.

Clinical pharmacology and therapeutics·2007
Same author

Factors associated with the initiation of alpha-interferon treatment in Medicaid patients diagnosed with hepatitis C.

Journal of viral hepatitis·2005
Same author

An explanation of the second-dose effect in pharmacokinetics and its meaning for clinical psychopharmacology.

Psychopharmacology bulletin·2002

This study monitored antidepressant drug interactions in 170 patients. Results showed fewer occult interactions than expected, suggesting newer antidepressants are safer when combined with other drugs.

Area of Science:

  • Pharmacology
  • Clinical Pharmacy
  • Psychiatric Therapeutics

Background:

  • Antidepressant drug interactions pose a risk to patient safety.
  • The cytochrome P-450 (CYP) enzyme system is crucial for metabolizing many drugs, including newer antidepressants.

Purpose of the Study:

  • To prospectively evaluate the occurrence and significance of metabolic drug interactions involving newer antidepressants.
  • To assess the prevalence of occult (undetected) drug interactions with selective serotonin reuptake inhibitors (SSRIs) and other newer antidepressants.

Main Methods:

  • A 4-year prospective surveillance program (Charleston Antidepressant Drug Interactions Surveillance Program, CADISP) enrolled 170 psychiatric patients.
  • Plasma concentrations and clinical effects of drug combinations were monitored in patients receiving SSRIs, nefazodone, or venlafaxine with other CYP-metabolized drugs.

Related Experiment Videos

  • Plasma drug concentrations, with and without antidepressant treatment, served as the primary assessment variable.
  • Main Results:

    • Little evidence of occult pharmacokinetic drug-drug interactions was found with newer antidepressants.
    • Commonly predicted drug interactions were documented, indicating some interactions do occur.
    • The study found that the feared prevalence and routine hazard of these interactions may be overestimated.

    Conclusions:

    • While caution is still warranted when prescribing antidepressants with potential for metabolic interactions, the data suggest these interactions are less prevalent and hazardous than often feared.
    • These findings help allay concerns about the routine clinical danger of drug interactions with newer antidepressants.
    • Further monitoring and research are needed to fully understand the clinical impact of antidepressant drug interactions.