Imidafenacin
Overview of the antimuscarinic drug Imidafenacin
Imidafenacin is a medication used primarily in the treatment of overactive bladder (OAB). It is classified as an antimuscarinic agent, which works by inhibiting the action of acetylcholine on muscarinic receptors in the bladder, thereby reducing urinary urgency, frequency, and incontinence.
Pharmacology[edit | edit source]
Imidafenacin is a selective antagonist for the M3 and M1 subtypes of muscarinic receptors. These receptors are predominantly found in the bladder and salivary glands. By blocking these receptors, imidafenacin reduces involuntary bladder contractions and increases bladder capacity.
Mechanism of Action[edit | edit source]
The mechanism of action of imidafenacin involves competitive inhibition of muscarinic receptors. This inhibition decreases the detrusor muscle contractions of the bladder, which are responsible for the symptoms of overactive bladder. The selectivity for M3 receptors helps in minimizing side effects such as dry mouth and constipation, which are common with non-selective antimuscarinics.
Clinical Use[edit | edit source]
Imidafenacin is indicated for the management of overactive bladder with symptoms of urgency, frequency, and urge incontinence. It is administered orally and is available in tablet form. The typical dosage is 0.1 mg twice daily, but the dosage may be adjusted based on patient response and tolerability.
Side Effects[edit | edit source]
Common side effects of imidafenacin include dry mouth, constipation, and blurred vision. These effects are due to its anticholinergic properties. Less common side effects may include urinary retention, dizziness, and headache.
Contraindications[edit | edit source]
Imidafenacin is contraindicated in patients with urinary retention, gastric retention, uncontrolled narrow-angle glaucoma, and in those who have demonstrated hypersensitivity to the drug or its components.
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