Abciximab contraindications: Difference between revisions

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* Recent (within six weeks) gastrointestinal (GI) or genitourinary (GU) bleeding of clinical significance.
* Recent (within six weeks) gastrointestinal (GI) or genitourinary (GU) bleeding of clinical significance.
* History of [[CVA|cerebrovascular accident (CVA)]] within two years, or [[CVA]] with a significant residual neurological deficit
* History of [[CVA|cerebrovascular accident (CVA)]] within two years, or [[CVA]] with a significant residual neurological deficit
* Bleeding diathesis
* [[Bleeding diathesis]]
* Administration of oral [[anticoagulant]]s within seven days unless [[prothrombin time]] is <1.2 times control
* Administration of oral [[anticoagulant]]s within seven days unless [[prothrombin time]] is <1.2 times control
* [[Thrombocytopenia]] (<100 000 cells/m L)
* [[Thrombocytopenia]] (<100 000 cells/m L)

Revision as of 17:16, 30 January 2014

Template:Abciximab Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sheng Shi, M.D. [2], Pratik Bahekar, MBBS [3]

Contraindications

Because Abciximab may increase the risk of bleeding, Abciximab is contraindicated in the following clinical situations:

References

  1. "REOPRO (ABCIXIMAB) INJECTION, SOLUTION [ELI LILLY AND COMPANY]".

Adapted from the FDA Package Insert.