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Dabigatran Etexilate Mesylate and Isoptin SR

Determining the interaction of Dabigatran Etexilate Mesylate and Isoptin SR and the possibility of their joint administration.

Check result:
Dabigatran Etexilate Mesylate <> Isoptin SR
Relevance: 08.12.2022 Reviewer: Shkutko P.M., M.D., in

In the database of official manuals used in the service creation an interaction registered by statistical results of studies was found, which can either lead to negative consequences for the patient health or strengthen a mutual positive effect. A doctor should be consulted to address the issue of joint drug administration.

Consumer:

Verapamil may increase the blood levels and effects of dabigatran. Combining these medications may increase the risk of anemia and bleeding complications. You may need a dose adjustment or more frequent monitoring by your doctor to safely use both medications. Call your doctor promptly if you experience paleness of skin, fatigue, dizziness, fainting, unusual bleeding or bruising, swelling, vomiting, blood in your urine or stools, headache, or weakness during treatment with these medications. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.

Professional:

MONITOR CLOSELY: Coadministration with potent inhibitors of P-glycoprotein such as verapamil may significantly increase the bioavailability of dabigatran following oral administration of dabigatran etexilate, which is a substrate of the efflux transporter. When dabigatran etexilate 150 mg was coadministered with oral verapamil, dabigatran peak plasma concentration (Cmax) and systemic exposure (AUC) increased, but the extent varied depending on the formulation of verapamil and timing of administration. Specifically, dabigatran Cmax and AUC increased by approximately 2.8- and 2.5-fold, respectively, when a single dose of immediate-release verapamil was given one hour prior to dabigatran etexilate. The effect was smaller with an extended release formulation of verapamil, which increased dabigatran Cmax by about 90% and AUC by about 70%. Administration of multiple doses of verapamil (120 mg twice a day for 3 days) increased dabigatran Cmax by about 60% and AUC by about 50%. In contrast, the increases in dabigatran Cmax and AUC were negligible (about 10% and 20%, respectively) when verapamil was given 2 hours after dabigatran etexilate, presumably because dabigatran absorption is complete after 2 hours. In a phase 3 clinical trial of dabigatran etexilate for the prevention of stroke and systemic embolism in patients with atrial fibrillation, no important changes in dabigatran trough levels were observed in patients who received verapamil. Annualized major bleeding rates in patients who had used verapamil at least once together with warfarin, dabigatran etexilate 110 mg twice daily or 150 mg twice daily were reported at 3.33 %, 3.09 % and 3.92%, respectively. No pharmacokinetic data are available for dabigatran during the parenteral administration of verapamil. However, based on the known mechanism of interaction, no meaningful interaction is expected.

MANAGEMENT: Caution is advised if dabigatran etexilate is prescribed in combination with oral verapamil. No dosage adjustment is recommended when dabigatran etexilate is used for the prevention of stroke and systemic embolism in patients with atrial fibrillation. However, some experts recommend reducing dabigatran etexilate dosage to 150 mg daily (normally 220 mg daily) when used for the prevention of venous thromboembolic events after hip- or knee-replacement surgery, although this is not an FDA-approved indication. In patients with moderate renal impairment, a further dosage reduction to 75 mg daily may be considered during concomitant treatment with oral verapamil. To minimize the potential for interaction, dabigatran etexilate should be administered at least two hours before verapamil in patients receiving the combination. In addition, patients should be monitored closely for the development of anemia and bleeding complications.

References
  • Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
  • "Product Information. Pradax (dabigatran)." Boehringer Ingelheim (Canada) Ltd, Burlington, IA.
  • "Product Information. Pradaxa (dabigatran)." Boehringer-Ingelheim, Ridgefield, CT.
  • Cerner Multum, Inc. "Australian Product Information." O 0
Dabigatran Etexilate Mesylate

Generic Name: dabigatran

Brand name: Pradaxa

Synonyms: Dabigatran, Dabigatran Etexilate

Isoptin SR

Generic Name: verapamil

Brand name: Calan SR, Isoptin SR, Calan, Verelan, Isoptin, Isoptin IV, Covera-HS, Verelan PM

Synonyms: n.a.

In the course of checking the drug compatibility and interactions, data from the following reference sources was used: Drugs.com, Rxlist.com, Webmd.com, Medscape.com.

Interaction with food and lifestyle