Details of Drug-Drug Interaction
| Drug General Information (ID: DDIPB7X9SR) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Warfarin | Drug Info | Heparin | Drug Info | |||||
| Drug Type | Small molecule | Small molecule | |||||||
| Therapeutic Class | Anticoagulants | Anticoagulants | |||||||
| Structure | |||||||||
| Mechanism of Warfarin-Heparin Interaction (Severity Level: Major) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Increased risk of bleeding Click to Show/Hide Mechanism Graph | |||||||||
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| Drug Name | Warfarin | Heparin | |||||||
| Mechanism |
Risk of bleeding Anticoagulant |
Risk of bleeding Anticoagulant |
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| Key Mechanism Factor 1 | |||||||||
| Factor Name | Bleeding | ||||||||
| Factor Description | Patients may be at risk for bleeding when the outcome of a disease or disease treatment confounds the standard mechanisms for maintaining hemostasis. Signs or symptoms of abnormal bleeding include: bleeding that takes a long time to stop (including nosebleeds, bleeding gums, bleeding from cuts and abrasions, and menstrual bleeding); severe unexplained bruising, or bruising that becomes larger; blood in the urine or stool, etc. | ||||||||
| Mechanism Description |
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| Recommended Action | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Management | During concurrent or overlapping therapy, close clinical and laboratory observation for hematologic complications is recommended. To minimize the interference of heparin on INR determinations, blood should not be drawn until at least 5 hours after the last intravenous heparin dose or 24 hours after the last subcutaneous heparin dose. | ||||||||
| References | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Product Information. Coumadin (warfarin). DuPont Pharmaceuticals, Wilmington, DE. | ||||||||||||||||||
| 2 | Product Information. Heparin Sodium (heparin). Lilly, Eli and Company, Indianapolis, IN. | ||||||||||||||||||

