Drug intelligence / Profile preview

warfarin + fesoterodine

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral
01

Overview

Warfarin + fesoterodine is a combination of two pharmaceutical agents, each with distinct mechanisms and indications. Warfarin is an oral anticoagulant that acts as a vitamin K antagonist, inhibiting the synthesis of vitamin K-dependent clotting factors (II, VII, IX, X) and proteins C and S. It is primarily used for the prevention and treatment of thromboembolic disorders such as venous thromboembolism, pulmonary embolism, atrial fibrillation-related stroke risk reduction, and prosthetic heart valve thromboprophylaxis[8]. Fesoterodine is an antimuscarinic agent indicated for the treatment of overactive bladder with symptoms including urge urinary incontinence, urgency, frequency in adults and neurogenic detrusor overactivity in pediatric patients[4][6]. Fesoterodine acts as a competitive antagonist at muscarinic acetylcholine receptors (M1–M5), reducing involuntary bladder contractions[4][5]. Clinical studies have shown no significant pharmacokinetic or pharmacodynamic interaction between warfarin and fesoterodine when co-administered; both drugs maintain their efficacy and safety profiles when used together[1][2][3][5].

Other names
warfarinfesoterodine
02

Targets

M1 (Muscarinic acetylcholine receptor M1)CHRM4 (M4)VKORC1 (Vitamin K epoxide reductase complex subunit 1)CHRM3 (M3)CHRM5 (M5)CHRM2 (M2)

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