Avanafil, product photo
Medication

Avanafil

Avanafil - the fastest of the PDE5 inhibitors. First successes from 15 minutes, a window beyond six hours.

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At a glance

Avanafil by the numbers

The key figures from our lexicon.

Full lexicon entry
Class
Second-generation PDE-5 inhibitor

Stendra, Spedra

Half-life
About 5 hours

US label, 6 to 17 hours (EU SmPC)

Use
Oral

on demand, about 15 to 30 minutes before, at most once in 24 hours

Sizes
100 to 200 mg

2 sizes in the shop

For research and educational purposes only. Values from the TPD lexicon, sources linked there.

There is no lab analysis for Avanafil yet. Vote for itAll lab analyses

Knowledge

Everything about Avanafil

Description

Avanafil is the most recent of the four PDE5 inhibitors and was developed around two properties: rapid onset and high selectivity. The mechanism is the same as for sildenafil, tadalafil and vardenafil. Phosphodiesterase type 5 breaks down cyclic guanosine monophosphate in erectile tissue; inhibit it and cGMP persists longer, smooth muscle relaxes and arterial inflow rises. As with the whole class, the substance only amplifies an existing signalling chain, it does not start a new one. Without sexual stimulation nothing happens.

The difference lies in the kinetics. The review by Sanford gives a median time to peak plasma concentration of 30 to 45 minutes, markedly shorter than the older members. In that analysis, roughly two thirds of attempts made either before 15 minutes or more than six hours after dosing were successful, against around one quarter on placebo.

The randomized, double-blind multicenter study by Goldstein and colleagues examined 390 men with diabetes mellitus and erectile dysfunction, allocated to 100mg, 200mg or placebo. Both doses improved all three co-primary endpoints significantly versus placebo. The timing held here as well: successful intercourse was possible from 15 minutes and still more than six hours after dosing. Diabetes is not an arbitrary subgroup but one of the harder ones, because a vascular and a neurogenic component often coincide.

High selectivity for PDE5 over PDE6 and PDE11 is the second point. PDE6 sits in the retina and is responsible for the visual disturbances seen with sildenafil; PDE11 is associated with muscle pain. The adverse effects reported most often in the trials were headache, nasopharyngitis, flushing and sinus congestion.

In a research context avanafil is therefore the member of the class with the shortest lead time and the most tolerable profile, but a distinctly shorter window than tadalafil.

You can order Avanafil as oral tablets with 100mg or 200mg per tablet, 4 tablets per blister.

This information is for research and educational purposes only. No medical advice.

Risks & Safety

The better tolerability profile changes nothing about the contraindication that applies to the entire class.

  • Nitrates are an absolute contraindication: Nitroglycerin, isosorbide dinitrate, isosorbide mononitrate and the alkyl nitrites sold as poppers. Nitrates and PDE5 inhibitors act on the same signalling chain. Together they can drop blood pressure to life-threatening levels. The faster onset of avanafil makes this point more dangerous rather than less, because less time passes between dosing and effect.
  • Alpha blockers and other antihypertensives: The effects add up. Relevant with tamsulosin and alfuzosin among others.
  • Cardiovascular status: Sexual activity is exertion. With unstable angina, a recent heart attack or stroke, or severe heart failure, capacity to exert is the real question.
  • Tolerability in the trials: In a pooled analysis of three trials, per Sanford, at most 2 percent of avanafil and placebo recipients discontinued because of adverse events. Across more than 52 weeks of continued use it was 2.8 percent, with no drug-related serious adverse events.
  • Common adverse effects: Headache, nasopharyngitis, flushing and sinus congestion, as reported by Goldstein and colleagues.
  • Visual disturbances and priapism: Not excluded despite the higher selectivity. Any sudden loss of vision and any erection lasting more than four hours is an emergency.
  • CYP3A4: Avanafil is metabolised via CYP3A4. Strong inhibitors such as ketoconazole, itraconazole, clarithromycin or ritonavir raise exposure substantially.

This classification does not replace medical advice. Risk and responsibility for any actual use lie entirely with the buyer.

Studies

Dosing

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FAQ

Frequently asked

Sources for every answer: lexicon entry

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How does avanafil work?

With arousal nerves in the erectile tissue release nitric oxide, the messenger cGMP rises and the vessels widen. PDE5 breaks cGMP down again. Avanafil inhibits PDE5 and the signal lasts longer. Without sexual stimulation the chain does not start.

How fast does it work?

Fasted, the peak level is reached after 30 to 45 minutes. In the stopwatch trial with 440 men the difference from placebo was significant from 10 to 12 minutes. In the registration trial 64 to 71 percent of attempts within 15 minutes succeeded, 27 percent with placebo. A high-fat meal pushes the peak back.

Is avanafil approved?

Yes. In the US since April 2012, ChEMBL lists it with phase 4 as the highest phase. ClinicalTrials.gov lists 24 trials, 7 of them completed phase 3 trials (as of 26 October 2026). Everything here is the state of research, not a recommendation.

What does the high selectivity mean?

In a lab comparison avanafil inhibited PDE6 in the retina 121-fold more weakly than PDE5, sildenafil and vardenafil only 16- to 21-fold. Over PDE1 the gap was more than 10,000-fold, over PDE11 more than 19,000-fold. Less binding to these off-targets suggests fewer visual disturbances and muscle pains, direct comparison trials are missing.

Does it also work in diabetes or after prostate surgery?

In both groups yes, at a lower level. In 390 men with diabetes intercourse succeeded in 34 to 40 percent of attempts at the end, 20.5 percent with placebo. After nerve-sparing prostate removal (298 men, mostly severe dysfunction) it was 23 to 26 versus 8.9 percent.

Why never with nitrates?

Nitrates and avanafil act on the same signalling chain, together blood pressure can fall to life-threatening levels. That also applies to poppers. The label requires at least 12 hours between the last dose and a nitrate in an emergency. Strong CYP3A4 inhibitors such as ketoconazole raise the level up to 13-fold.

What did the long-term trial show?

712 men continued avanafil open-label for 52 weeks. At the middle dose the share of successful attempts rose from 13 to 68 percent. Of the men for whom the middle dose was not enough, 65 percent responded to the highest. Fewer than 3 percent stopped because of side effects.

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