Clinically proven PDE5 inhibitor. Discreet, doctor-supervised, delivered to your door. No awkward pharmacy visits. No judgment.
Sildenafil's mechanism targets the vascular system to improve erectile function through a well-understood biochemical pathway. It works by enhancing the body's natural responses to sexual stimulation.
Sildenafil achieves ~41% oral bioavailability with rapid absorption. Peak plasma concentration occurs 30–120 minutes post-dose (faster on empty stomach). The active N-desmethyl-sildenafil metabolite contributes ~50% of the pharmacological activity. CYP3A4 metabolism is critical—inhibitors can double or triple sildenafil levels, creating safety concerns.
| Bioavailability | ~41% (oral) |
| Tmax (time to peak) | 30–120 minutes (variable with food/stomach) |
| Peak concentration (50mg dose) | ~1 µg/mL |
| Elimination half-life | 3–5 hours |
| Volume of distribution | ~1.6 L/kg |
| Protein binding | ~96% — highly protein-bound |
| Metabolism | Hepatic: CYP3A4 (major, ~70%), CYP2C9 (minor, ~20%). Critical—CYP3A4 inhibitors dramatically increase levels. |
| Active metabolite | N-desmethyl-sildenafil (~50% activity of parent). Contributes to prolonged duration. |
| Excretion | Fecal (~80%), renal (~13%). Minimal unchanged parent in urine. |
| Food effect | High-fat meal delays Tmax by ~60 min and reduces Cmax by ~29%. Empty stomach optimal. |
Sildenafil is dosed as needed, 25–100mg taken 30–60 minutes before sexual activity. Maximum once daily. Standard starting dose is 50mg. Standard approach is flexible dosing based on response and tolerability, not daily maintenance dosing.
Sildenafil is one of the most-studied medications in history with robust evidence spanning erectile dysfunction, cardiovascular performance, and athletic enhancement. Over 25 years of clinical data support safety and efficacy.
Sildenafil's side effect profile is well-characterized from decades of use in millions of men. Most effects are mild, reversible, and dose-dependent. At standard doses (25–100mg), serious adverse events are rare.
Sildenafil is metabolized by CYP3A4 and CYP2C9. CYP3A4 inhibitors can substantially increase sildenafil levels (2–10x), creating safety risks. Nitrates are an absolute contraindication. Your physician MUST review all medications.
Book a consultation with a licensed physician to discuss whether sildenafil is appropriate for you.