Tadalafil
PEPTIDES+ MEMBERS ONLY
INDICATIONS FOR USE
Tadalafil is FDA-approved for the treatment of erectile dysfunction (ED), benign prostatic hyperplasia (BPH), and pulmonary arterial hypertension (PAH). It is also used off-label to manage conditions such as Raynaud’s phenomenon and endothelial dysfunction.
ROUTE OF ADMINISTRATION
Administered orally in tablet or troche form.
FORMULATIONS AND PRICING
Formulation | Price |
---|---|
20mg troche (#15/#30) | $47 / $75 |
40mg troche (#15/#30) | $47 / $75 |
COMMON INITIAL DOSING REGIMENS
For Erectile Dysfunction: An initial dose of 10 mg taken orally before anticipated sexual activity is common, with a maximum frequency of once per day. For daily use, a lower dose of 2.5–5 mg is recommended, irrespective of timing of sexual activity.
MECHANISM OF ACTION
Tadalafil is a selective phosphodiesterase type 5 (PDE5) inhibitor. By inhibiting PDE5, tadalafil prevents the breakdown of cyclic guanosine monophosphate (cGMP) in the smooth muscle cells of the corpus cavernosum, pulmonary vasculature, and other vascular tissues.
In ED, increased cGMP levels result in enhanced smooth muscle relaxation and increased blood flow to the penis during sexual stimulation, promoting erection.
Tadalafil is distinguished by its long half-life (17.5 hours), which provides a prolonged duration of action, often referred to as the “weekend pill.”
COMMON SIDE EFFECTS
Cardiovascular: Headache, flushing, and dizziness are common due to systemic vasodilation. Hypotension and tachycardia may occur but are less common.
Gastrointestinal: Dyspepsia, nausea, and abdominal pain.
Musculoskeletal: Back pain and myalgia are unique side effects of tadalafil, possibly related to PDE11 inhibition.
Respiratory: Nasal congestion.
Rare but Severe: Non-arteritic anterior ischemic optic neuropathy (NAION), sudden hearing loss, and priapism (prolonged erection requiring medical attention).
CONTRAINDICATIONS
Absolute: Hypersensitivity to finasteride or any excipient in the formulation. Pregnant or potentially pregnant women should not handle finasteride-containing products due to the risk of absorption and potential harm to a male fetus.
Relative: Patients with significant scalp irritation or broken skin should use topical finasteride cautiously to avoid increased systemic absorption. Use in women for androgenetic alopecia remains off-label and requires careful consideration.
ADDITIONAL NOTES ON EFFICACY
Absolute: Concurrent use with nitrates (e.g., nitroglycerin) or guanylate cyclase stimulators (e.g., riociguat) due to the risk of severe hypotension. Hypersensitivity to tadalafil or any excipient.
Relative: Use cautiously in individuals with severe hepatic or renal impairment, severe cardiovascular conditions, significant hypotension (<90/50 mmHg), or a recent history of stroke or myocardial infarction. Patients with retinitis pigmentosa or predisposing conditions for priapism (e.g., sickle cell anemia, multiple myeloma, leukemia) require additional caution.
COMPARISON WITH SILDENAFIL
Tadalafil has a longer half-life (17.5 hours) compared to sildenafil (4–6 hours), allowing for greater flexibility with dosing and a prolonged therapeutic window. This makes tadalafil suitable for daily dosing and sustained effects (“weekend pill”).
Tadalafil also has unique efficacy in managing BPH, which sildenafil does not address. Both medications share similar side effects, but tadalafil has a distinct risk of musculoskeletal pain.
MORE INFORMATION
FDA Safety Data Sheet for tadalafil may be found here.