section name header

Pronunciation

tam-SOO-loe-sin

Classifications

Therapeutic Classification: benign prostatic hyperplasia bph agents

Pharmacologic Classification: alpha adrenergic blockers

Indications

REMS


Action

  • Decreases contractions in smooth muscle of the prostatic capsule by preferentially binding to alpha1-adrenergic receptors.
Therapeutic effects:
  • Decreased symptoms of BPH (urinary urgency, hesitancy, nocturia).

Pharmacokinetics

Absorption: >90% absorbed after oral administration.

Distribution: Widely distributed to tissues.

Protein Binding: 94–99%.

Metabolism/Excretion: Primarily metabolized by the liver via the CYP3A4 and CYP2D6 isoenzymes; the CYP2D6 enzyme system exhibits genetic polymorphism (7% of population may be poor metabolizers and may have significantly tamsulosin concentrations and an risk of adverse effects).<10% excreted unchanged in urine.

Half-Life: 14 hr.

Time/Action Profile

( in urine flow)
ROUTEONSETPEAKDURATION
POunknown2 wkunknown



Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: orthostatic hypotension

EENT: intraoperative floppy iris syndrome, rhinitis

GU: priapism, retrograde/diminished ejaculation

Neuro: dizziness, headache

Interactions

Drug-drug:

Route/Dosage

Availability

(Generic available)

Assessment

Implementation

Patient/Family Teaching

Evaluation/Desired Outcomes

US Brand Names

Flomax

Canadian Brand Names

Flomax CR

Pill Image

tamsulosin_195-8336.jpg