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Omeprazole: a possible new candidate influencing the antiplatelet effect of clopidogrel.

Publication ,  Journal Article
Gurbel, PA; Lau, WC; Tantry, US
Published in: J Am Coll Cardiol
January 22, 2008

Duke Scholars

Published In

J Am Coll Cardiol

DOI

EISSN

1558-3597

Publication Date

January 22, 2008

Volume

51

Issue

3

Start / End Page

261 / 263

Location

United States

Related Subject Headings

  • Ticlopidine
  • Stents
  • Proton Pump Inhibitors
  • Polymorphism, Genetic
  • Platelet Aggregation Inhibitors
  • Omeprazole
  • Mixed Function Oxygenases
  • Humans
  • Drug Therapy, Combination
  • Drug Antagonism
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Gurbel, P. A., Lau, W. C., & Tantry, U. S. (2008). Omeprazole: a possible new candidate influencing the antiplatelet effect of clopidogrel. J Am Coll Cardiol, 51(3), 261–263. https://doi.org/10.1016/j.jacc.2007.07.090
Gurbel, Paul A., Wei C. Lau, and Udaya S. Tantry. “Omeprazole: a possible new candidate influencing the antiplatelet effect of clopidogrel.J Am Coll Cardiol 51, no. 3 (January 22, 2008): 261–63. https://doi.org/10.1016/j.jacc.2007.07.090.
Gurbel PA, Lau WC, Tantry US. Omeprazole: a possible new candidate influencing the antiplatelet effect of clopidogrel. J Am Coll Cardiol. 2008 Jan 22;51(3):261–3.
Gurbel, Paul A., et al. “Omeprazole: a possible new candidate influencing the antiplatelet effect of clopidogrel.J Am Coll Cardiol, vol. 51, no. 3, Jan. 2008, pp. 261–63. Pubmed, doi:10.1016/j.jacc.2007.07.090.
Gurbel PA, Lau WC, Tantry US. Omeprazole: a possible new candidate influencing the antiplatelet effect of clopidogrel. J Am Coll Cardiol. 2008 Jan 22;51(3):261–263.
Journal cover image

Published In

J Am Coll Cardiol

DOI

EISSN

1558-3597

Publication Date

January 22, 2008

Volume

51

Issue

3

Start / End Page

261 / 263

Location

United States

Related Subject Headings

  • Ticlopidine
  • Stents
  • Proton Pump Inhibitors
  • Polymorphism, Genetic
  • Platelet Aggregation Inhibitors
  • Omeprazole
  • Mixed Function Oxygenases
  • Humans
  • Drug Therapy, Combination
  • Drug Antagonism