Integrilin Disease Interactions
There are 2 disease interactions with Integrilin (eptifibatide).
Eptifibatide (applies to Integrilin) renal dysfunction
Major Potential Hazard, High plausibility.
The use of eptifibatide is contraindicated in patients dependent of dialysis. Approximately 50% of eptifibatide is cleared by the kidney in patients with normal renal function. Total drug clearance is decreased by approximately 50% and steady-state plasma eptifibatide concentrations are doubled in patients with an estimated CrCl <50 mL/min. Therefore, the infusion dose should be reduced to 1 mcg/kg/min in such patients Clinical monitoring of renal function is recommended.
References (1)
- (2001) "Product Information. Integrilin (eptifibatide)." Schering Corporation
GpIIb/IIIa platelet inhibitors (applies to Integrilin) bleeding risks
Major Potential Hazard, High plausibility. Applicable conditions: Brain/Intracranial Tumor, Thrombocytopathy, Cerebral Vascular Disorder, Hypertension, Coagulation Defect, Thrombocytopenia
The use of gp11b/111a platelet inhibitors is contraindicated in patients with active internal bleeding, recent significant gastrointestinal or genitourinary bleeding (within 6 weeks), recent trauma or major surgery (within 6 weeks), history of bleeding diathesis, recent stroke (within 4 weeks), history of hemorrhage stroke or residual neurologic deficit, intracranial defect (aneurysm, arteriovenous malformation, neoplasm), uncontrolled hypertension (SBP > 180; DBP > 110), or thrombocytopenia (<100,000/mm3). Thrombocytopenia, serious GI/GU bleeding, hemorrhagic retinopathy, and bleeding at the arterial access have been reported during gp11b/111a platelet inhibitor therapy. Clinical monitoring of hemoglobin and hematocrit (H/H), platelet count, prothrombin time (PT) and activated partial prothrombin time (aPTT) is recommended prior to initiation of, during and following gp11b/111a platelet inhibitor therapy.
References (9)
- Landefeld CS, Cook EF, Flatley M, Weisberg M, Goldman L (1987) "Identification and preliminary validation of predictors of major bleeding in hospitalized patients starting anticoagulant therapy." Am J Med, 82, p. 703-13
- Boehrer JD, Kereiakes DJ, Navetta FI, Califf RM, Topol EJ (1994) "Effects of profound platelet inhibition with c7E3 before coronary angioplasty on complications of coronary bypass surgery." Am J Cardiol, 74, p. 1166-70
- Kereiakes DJ, Essell JH, Abbottsmith CW, Broderick TM, Runyon JP (1996) "Abciximab-associated profound thrombocytopenia: therapy with immunoglobulin and platelet transfusion." Am J Cardiol, 78, p. 1161
- (2001) "Product Information. Aggrastat (tirofiban)." Merck & Co., Inc
- Adgey AA (1998) "An overview of the results of clinical trials with glycoprotein IIb/IIIa inhibitors." Am Heart J, 135, s43-55
- Kleiman NS (1997) "Primary and secondary safety endpoints from IMPACT II. Integrilin to Minimize Platelet Aggregation and Coronary Thrombosis." Am J Cardiol, 80, b29-33
- The IMPACT-II Investigators (1997) "Randomised placebo-controlled trial of effect of eptifibatide on complications of percutaneous coronary intervention: IMPACT-II." Lancet, 349, p. 1422-8
- The RESTORE Investigators (1997) "Effects of platelet glycoprotein IIb/IIIa blockade with tirofiban on adverse cardiac events in patients with unstable angina or acute myocardial infarction..." Circulation, 96, p. 1445-53
- (2001) "Product Information. Integrilin (eptifibatide)." Schering Corporation
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Integrilin drug interactions
There are 149 drug interactions with Integrilin (eptifibatide).
Integrilin alcohol/food interactions
There is 1 alcohol/food interaction with Integrilin (eptifibatide).
More about Integrilin (eptifibatide)
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- Drug class: glycoprotein platelet inhibitors
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Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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