section name header

Pronunciation ⬇

so-li-FEN-a-sin

Classifications ⬆ ⬇

Therapeutic Classification: urinary tract antispasmodics

Pharmacologic Classification: anticholinergics

Indications ⬆ ⬇

REMS


Action ⬆ ⬇

  • Acts as a muscarinic (cholinergic) receptor antagonist; antagonizes bladder smooth muscle contraction.
Therapeutic effects:
  • Decreased symptoms of overactive bladder.
  • Improved maximum cystometric capacity in neurogenic detrusor overactivity.

Pharmacokinetics ⬆ ⬇

Absorption: 90% absorbed following oral administration.

Distribution: Extensively distributed to tissues.

Protein Binding: 98%.

Metabolism/Excretion: Extensively metabolized by liver via the CYP3A4 isoenzyme. 69% excreted in urine as metabolites, 22% in feces.

Half-Life: Tablets: 45–68 hr.

Time/Action Profile ⬆ ⬇

(plasma concentrations)

ROUTEONSETPEAKDURATION
Oralunknown3–8 hr24 hr



Contraind./Precautions ⬆ ⬇

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects ⬆ ⬇

CV: palpitations, QT interval prolongation, tachycardia

EENT: blurred vision

GI: constipation, dry mouth, abdominal pain, dyspepsia, nausea

GU: urinary tract infection

MS: muscle weakness

Neuro: confusion, drowsiness, hallucinations, headache

Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS AND ANGIOEDEMA)

Interactions ⬆ ⬇

Drug-drug:

Route/Dosage ⬆ ⬇

Overactive Bladder

Renal Impairment

Hepatic Impairment

Availability ⬆ ⬇

(Generic available)

Assessment ⬆ ⬇

Implementation ⬆ ⬇

Patient/Family Teaching ⬆ ⬇

Evaluation/Desired Outcomes ⬆ ⬇

US Brand Names ⬆

VESIcare