Tadalafil
Tadalafil is a PDE5 (phosphodiesterase type 5) inhibitor FDA-approved for erectile dysfunction, benign prostatic hyperplasia (BPH), and pulmonary arterial hypertension. Its 36-hour half-life distinguishes it from sildenafil (Viagra, 4-5h) — allowing the "weekend pill" or daily low-dose (5mg) dosing strategies. Beyond sexual function, daily tadalafil has growing evidence for: improved exercise tolerance, reduced blood pressure, anti-inflammatory effects via cGMP pathway, potential neuroprotection, and cardiovascular benefits. At 5mg/day it is FDA-approved for both ED and BPH, and is widely used off-label as part of longevity and cardiovascular optimization protocols.
Evidence
No score yet
Safety
Unknown safety profile
Clinical Status
No formal phase listed
Research Sync
Not synced yet
Dosing
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Pharmacology
Evidence Score
Plain-English Snapshot
Tadalafil is currently categorized as a hormonal compound.
Evidence scoring has not been fully computed yet, so interpret this profile as preliminary.
Safety scoring is incomplete. Start conservatively and monitor carefully.
Core mechanism
Selective PDE5 inhibitor; prevents cGMP degradation in vascular smooth muscle → eNOS-derived NO maintains vasodilation → sustained vasodilation in penile corpus cavernosum, pulmonary vasculature, prostate
Practical Context
Strongest current signals
No indexed study summaries yet.
Elevated caution signals
1 severe/high side effect flag