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Not medical advice. The Atlas is not a substitute for a clinician who can examine you.

Avanafil

Stendra / Spedra (Avanafil)

Evidence grade 5 of 5, Settled. Read how the Atlas grades evidence.

The written rationale for this grade is still being prepared.

FDA
FDA Approved (2012)

Reference only. Not medical advice.

What can go wrong

Absolute contraindication with nitrates due to risk of severe hypotension. Common effects include headache, flushing, nasal congestion, and back pain. Caution with alpha-blockers and potent CYP3A4 inhibitors. Like all PDE5 inhibitors, rare reports of priapism and non-arteritic anterior ischemic optic neuropathy exist.

This is something to take to a clinician. The Atlas can tell you what is known about avanafil in general. It cannot tell you what is happening in your body, and the difference matters most for exactly the symptoms that bring people to this page.

Avanafil is the newest FDA-approved oral PDE5 inhibitor, cleared in April 2012 under the brand Stendra (Spedra in Europe). Its selling point is speed: many men achieve usable erections within about 15 minutes, and it is labeled for use as little as 15-30 minutes before intercourse. Its high PDE5 selectivity is intended to reduce visual and other off-target effects seen with older agents.

The fastest-acting PDE5 inhibitor on the US market.

What people take it for

What it is taken for. Approval, where it exists, covers only some of these.

  • Erectile dysfunction
  • On-demand use when rapid onset is desired

How it works

Like other PDE5 inhibitors, avanafil blocks phosphodiesterase type 5, preventing breakdown of cyclic GMP in penile smooth muscle so that nitric-oxide-driven vasodilation and erection are sustained in response to arousal. Its rapid absorption and high selectivity for PDE5 over PDE6 (retina) and other isoforms underlie its fast onset and comparatively favorable visual side-effect profile.

What people get wrong

  • Often saidAvanafil is stronger than Viagra

    ActuallyIt is faster and more PDE5-selective, not more potent; all PDE5 inhibitors enable rather than force an erection and require sexual stimulation.

Who profits, and who pushes back

Nobody is named here yet, because we have not done that work on this entry. Read that as unfinished. Somebody almost certainly sells this, and somebody almost certainly disputes it. Assume both until we have checked.

Set against the alternatives

Avanafil's main differentiator versus sildenafil and tadalafil is onset speed and PDE5 selectivity; it does not offer tadalafil's long duration or daily-dosing option. It remains less prescribed than generic sildenafil and tadalafil largely on cost.

Avanafil~15-30 min onset~5 h half-lifeFDA approved 2012
Sildenafil30-60 min onset~4 h half-lifeFDA approved 1998
Tadalafil30-45 min onset~17.5 h half-lifeFDA approved 2003

At a glance

FDA approval
2012
Onset
~15-30 minutes
Half-life
~5 hours
Doses
50, 100, 200 mg
Class
PDE5 inhibitor

What this entry does not yet cover

What follows is unfinished work on our side, not a finding about Avanafil. A short entry is not a safe entry.

  • Cost and market. We have not documented what it sells for or who sells it.
  • Supply chain. We have not mapped where it is made.
  • Who uses it. We have not documented the user groups.
  • What could change. No forward-looking summary yet.
  • Children and teenagers. We have not checked what is known about younger people.
  • Where we land. We have not taken a position on this yet.

Sources

The studies below are named and described, but not linked. You cannot open them from here and check our reading against them, which means this page is our summary of the literature rather than a document you can verify. Weigh it accordingly until the links exist.

The studies that matter

  • REVIVE trial2012

    Avanafil significantly improved erectile function versus placebo in general ED population

  • REVIVE-Diabetes2012

    Demonstrated efficacy in men with diabetes mellitus

  • Pooled rapid-onset analysis2013

    Subset of men responded to intercourse attempts ~15 minutes after dosing