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See the DrugPatentWatch profile for Flomax
Flomax (tamsulosin) mechanism of action: - It is a selective antagonist of alpha-1 adrenergic receptors, mainly α1A and α1D subtypes. - These receptors are abundant in the smooth muscle of the prostate, bladder neck, and urethra. - By blocking α1A/α1D, tamsulosin relaxes the smooth muscle in the bladder outlet and prostatic urethra, reducing urethral resistance and improving urine flow. - It does not shrink the prostate or treat the underlying cause of BPH; it relieves the dynamic component of obstruction. - Because it is relatively selective for α1A/α1D over α1B (which is more vascular), it tends to cause less orthostatic hypotension than nonselective alpha blockers, though fainting/dizziness can still occur, especially with the first dose.
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