Avanafil interactions
Full monograph for AvanafilCheck it against another medicine
Medicines
168 documented
Mechanism
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Aprepitant | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Ceritinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| CiprofloxacinbaseOphthalmic | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Ciprofloxacin + Dexamethasone | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme.2 documented mechanisms | 16 sources — open the full entry |
| Ciprofloxacin + Hydrocortisone Acetate | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Clarithromycin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Crizotinib | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Diltiazem Hydrochloride | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| ErythromycinLotionOral | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Esomeprazole + Amoxicillin + Clarithromycin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Finasteride + Tadalafil | Major | Synergy | The safety and efficacy of combining a phosphodiesterase-5 (PDE5) inhibitor with other PDE-5 inhibitors or other treatments for erectile dysfunction have not… | 9 sources — open the full entry |
| FluconazolebaseOphthalmic | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Imatinib Mesylate | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Isosorbide Dinitrate + Hydralazine Hydrochloride | Major | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the hypotensive effect of organic nitrates. Severe hypotension, syncope, or myocardial ischemia may result…2 documented mechanisms | 9 sources — open the full entry |
| Isosorbide Mononitrate | Major | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the hypotensive effect of organic nitrates. Severe hypotension, syncope, or myocardial ischemia may result… | 5 sources — open the full entry |
| Itraconazole | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Ketoconazole | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Ketoconazole + Zinc Pyrithione + Aleovera | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Lansoprazole + Amoxicillin + Clarithromycin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Lopinavir + Ritonavir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Mifepristone | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Mifepristone + Misoprostol | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Nelfinavir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Nirmatrelvir + Ritonavir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| NitroglycerinbaseIV InfusionOintment | Major | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the hypotensive effect of organic nitrates. Severe hypotension, syncope, or myocardial ischemia may result… | 5 sources — open the full entry |
| Posaconazole | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Rabeprazole + Amoxicillin + Clarithromycin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Ribociclib | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Sildenafil Citrate | Major | Synergy | The safety and efficacy of combining a phosphodiesterase-5 (PDE5) inhibitor with other PDE-5 inhibitors or other treatments for erectile dysfunction have not… | 9 sources — open the full entry |
| Tadalafil | Major | Synergy | The safety and efficacy of combining a phosphodiesterase-5 (PDE5) inhibitor with other PDE-5 inhibitors or other treatments for erectile dysfunction have not… | 9 sources — open the full entry |
| Tucatinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Vardenafil | Major | Synergy | The safety and efficacy of combining a phosphodiesterase-5 (PDE5) inhibitor with other PDE-5 inhibitors or other treatments for erectile dysfunction have not… | 9 sources — open the full entry |
| Verapamil Hydrochloride | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 3A4 may increase the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 6 sources — open the full entry |
| Vericiguat | Major | Synergy | Coadministration of vericiguat and phosphodiesterase type 5 (PDE-5) inhibitors may result in additive hypotension. PDE-5 inhibitors prevent degradation of… | 10 sources — open the full entry |
| Vonoprazan + Amoxicillin + Clarithromycin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Voriconazole | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Abametapir | Moderate | Metabolism | Based on in vitro inhibition data, a single topical application of abametapir lotion may increase plasma concentrations of drugs that are substrates of CYP450… | 1 sources — open the full entry |
| Acetazolamide | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated… | 4 sources — open the full entry |
| Alfuzosin Hydrochloride | Moderate | Synergy | Avanafil may potentiate the hypotensive effect of alpha blockers, resulting in symptomatic hypotension in some patients. Avanafil inhibits… | 6 sources — open the full entry |
| Ambrisentan | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated… | 4 sources — open the full entry |
| Amlodipine Besilate | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated… | 4 sources — open the full entry |
| Amlodipine Besilate + Atenolol | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated…2 documented mechanisms | 4 sources — open the full entry |
| Amlodipine Besilate + Atorvastatin | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated… | 4 sources — open the full entry |
| Amlodipine Besilate + Benazepril Hydrochloride | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated…2 documented mechanisms | 4 sources — open the full entry |
| Amlodipine Besilate + Olmesartan Medoxomil | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated…2 documented mechanisms | 4 sources — open the full entry |
| Amlodipine Besilate + Telmisartan | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated…2 documented mechanisms | 4 sources — open the full entry |
| Amlodipine Besilate + Valsartan | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated…2 documented mechanisms | 4 sources — open the full entry |
| Apalutamide | Moderate | Metabolism | Theoretically, coadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of avanafil, which is primarily metabolized by the isoenzyme. | 10 sources — open the full entry |
| Asciminib | Moderate | Metabolism | Coadministration with asciminib may increase the plasma concentrations of drugs that are primarily metabolized by the CYP450 3A4 isoenzyme. The mechanism is… | 1 sources — open the full entry |
| Atenolol | Moderate | Synergy | Phosphodiesterase-5 (PDE5) inhibitors may potentiate the blood pressure-lowering effect of antihypertensive medications. These agents inhibit PDE5-mediated… | 4 sources — open the full entry |
Food & lifestyle
alcohol
ModerateSynergy
Additive hypotensive effects may occur when phosphodiesterase-5 (PDE5) inhibitors are used with alcohol, as both are mild systemic vasodilators.
What to do: Patients taking avanafil should avoid consuming large amounts of alcohol, which may increase the potential for orthostatic signs and symptoms including increase in heart rate, decrease in standing blood pressure, dizziness, and headache. It may also be appropriate to avoid consuming large amounts of grapefruit juice. Some authorities advise that grapefruit juice should be avoided within 24 hours prior to taking avanafil.
5 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
Conditions
Conditions in which Avanafil needs care, as documented in this source.
Cardiovascular Diseases
MajorThe use of phosphodiesterase-5 (PDE5) inhibitors is not recommended in patients with preexisting cardiovascular disease for whom sexual activity is inadvisable due to the potential cardiac risk. Physicians should also consider the vasodilatory effect of these drugs and whether they may adversely affect patients with underlying cardio- and/or cerebrovascular conditions, in particular those who have suffered a myocardial infarction, stroke, or life-threatening arrhythmia within the last 6 months; those with resting hypotension (BP < 90/50) or hypertension (BP > 170/110); and those with unstable angina associated with cardiac failure or coronary artery disease. There are no controlled clinical data on the safety or efficacy in such patients. Other adverse cardiovascular effects reported include angina pectoris, myocardial infarction, AV block, ventricular arrhythmia, tachycardia, palpitation, hypotension, postural hypotension, syncope, cerebral thrombosis, cerebrovascular hemorrhage, transient ischemic attack, cardiac arrest, heart failure, and hypertension. Many of these events occurred in patients with cardiovascular risk factors and during or shortly after sexual activity.
19 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- Feenstra J, vanDriePierik RJHM, Lacle CF, Stricker BHC "Acute myocardial infarction associated with sildenafil." Lancet 352 (1998): 957-8
- Goldenberg MM "Safety and efficacy of sildenafil citrate in the treatment of male erectile dysfunction." Clin Ther 20 (1998): 1033-48
- Zusman RM "Cardiovascular data on sildenafil citrate - Introduction." Am J Cardiol 83 (1999): c1-2
- Conti CR, Pepine CJ, Sweeney M "Efficacy and safety of sildenafil citrate in the treatment of erectile dysfunction in patients with ischemic heart disease." Am J Cardiol 83 (1999): c29-34
- Zusman RM, Morales A, Glasser DB, Osterloh IH "Overall cardiovascular profile of sildenafil citrate." Am J Cardiol 83 (1999): c35-44
- Montorsi F, McDermott TED, Morgan R, Olsson A, Schultz A, Kirkeby HJ, Osterloh IH "Efficacy and safety of fixed-dose oral sildenafil in the treatment of erectile dysfunction of various etiologies." Urology 53 (1999): 1011-8
- Kloner RA, Zusman RM "Cardiovascular effects of sildenafil citrate and recommendations for its use." Am J Cardiol 84 (1999): n11-7
Show all 19 sourcesShow fewer sources
- Awan GM, Calderon E, Dawood G, Alpert MA "Acute, symptomatic atrial fibrillation after sildenafil citrate therapy in a patient with hypertrophic obstructive cardiomyopathy." Am J Med Sci 320 (2000): 69-71
- Kloner RA "Cardiovascular risk and sildenafil." Am J Cardiol 86 (2000): f57-61
- Moreira SG, Brannigan RE, Spitz A, Orejuela FJ, Lipshultz LI, Kim ED "Side-effect profile of sildenafil citrate (Viagra) in clinical practice." Urology 56 (2000): 474-6
- McMahon CG, Smali R, Johnson H "Efficacy, safety and patient acceptance of sildenafil citrate as treatment for erectile dysfunction." J Urol 164 (2000): 1192-6
- Malozowski S, Sahlroot JT "Hemodynamic effects of sildenafil." N Engl J Med 343 (2000): 967-8
- Dunn N "Cardiovascular events in users of sildenafil - Paper does not provide any reassurance." Br Med J 323 (2001): 50-1
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- Curran M, Keating G "Tadalafil." Drugs 63 (2003): 2203-12; discussion 2213-4
- Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
Kidney Diseases
MajorThe plasma clearance of phosphodiesterase-5 (PDE5) inhibitors may be decreased in patients with severe renal impairment, resulting in drug accumulation. Therapy with these agents should be avoided in patients with severe renal disease or on renal dialysis. Dose adjustments might be needed based on individual renal assessment and tolerability if used in these patients.
7 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
- "Product Information. Staxyn (vardenafil)." Merck & Co., Inc (2014):
Alcoholism
ModerateAlcohol consumption may intensify the pressure-lowering effects of mild vasodilators, such as phosphodiesterase 5 (PDE5) inhibitors. Therefore, patients that consume alcohol should be warned to limit alcohol intake while receiving these agents.
7 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
- "Product Information. Staxyn (vardenafil)." Merck & Co., Inc (2014):
Epilepsy
ModerateThe use of phosphodiesterase 5 (PDE-5) inhibitors has been associated with seizures. Therapy with these agents should be administered cautiously in patients with preexisting seizure disorders.
7 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
- "Product Information. Staxyn (vardenafil)." Merck & Co., Inc (2014):
Hearing Loss
ModerateUse of phosphodiesterase-5 (PDE5) inhibitors has been associated with sudden decrease or loss of hearing, which may be accompanied by tinnitus or dizziness. Patients with hearing problems should stop taking these agents and seek prompt medical care.
7 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
- "Product Information. Staxyn (vardenafil)." Merck & Co., Inc (2014):
Liver Diseases
ModeratePhosphodiesterase 5 (PDE-5) inhibitors are cleared predominantly by hepatic metabolism. The pharmacokinetic disposition of these agents has not been assessed in patients with severe hepatic impairment. No dosage modification is recommended for patients with mild to moderate hepatic impairment, however, therapy with these agents should not be administered to patients with severe hepatic impairment. In patients with mild hepatic impairment a lower dose of these agents should be used as initial therapy.
5 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
Priapism
ModerateProlonged erection greater than 4 hours and priapism (painful erections greater than 6 hours) have been reported during treatment with phosphodiesterase-5 (PDE 5) inhibitors. Priapism may result in penile tissue damage and permanent loss of potency if not treated promptly. These agents should be used cautiously in patients with conditions that may predispose them to priapism such as sickle cell anemia, multiple myeloma, or leukemia, and those with anatomical deformation of the penis (such as angulation, cavernosal fibrosis, or Peyronie's disease). If an erection persists longer than 4 hours, the patient should seek immediate medical assistance.
8 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- Kassim AA, Fabry ME, Nagel RL "Acute priapism associated with the use of sildenafil in a patient with sickle cell trait." Blood 95 (2000): 1878-9
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
- "Product Information. Staxyn (vardenafil)." Merck & Co., Inc (2014):
Retinitis Pigmentosa
ModeratePhosphodiesterase-5 (PDE5) inhibitors have been associated with transient impairment of color discrimination (blue/green) and blue- or color-tinged vision. These agents also inhibit phosphodiesterase-6 (PDE6), to a much lesser extent, which is involved in phototransduction in the retina. There are no controlled clinical data on the safety in patients with retinitis pigmentosa, a minority of whom may have genetic disorders of retinal phosphodiesterases. Therapy with these agents should be avoided in such patients.
15 sources
- "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals (2001):
- Goldstein I, Lue TF, Padma-Nathan H, Rosen RC, Steers WD, Wicker PA "Oral sildenafil in the treatment of erectile dysfunction." N Engl J Med 338 (1998): 1397-404
- Goldenberg MM "Safety and efficacy of sildenafil citrate in the treatment of male erectile dysfunction." Clin Ther 20 (1998): 1033-48
- Zrenner E "No cause for alarm over retinal side-effects of sildenafil." Lancet 353 (1999): 340-1
- Vobig MA, Klotz T, Staak M, BartzSchmidt KU, Engelmann U, Walter P "Retinal side-effects of sildenafil." Lancet 353 (1999): 375
- Marmor MF "Sildenafil (Viagra) and ophthalmology." Arch Ophthalmol 117 (1999): 518-9
- Montorsi F, McDermott TED, Morgan R, Olsson A, Schultz A, Kirkeby HJ, Osterloh IH "Efficacy and safety of fixed-dose oral sildenafil in the treatment of erectile dysfunction of various etiologies." Urology 53 (1999): 1011-8
- Vobig MA "Retinal side-effects of sildenafil." Lancet 353 (1999): 1442
Show all 15 sourcesShow fewer sources
- McMahon CG, Smali R, Johnson H "Efficacy, safety and patient acceptance of sildenafil citrate as treatment for erectile dysfunction." J Urol 164 (2000): 1192-6
- "Product Information. Levitra (vardenafil)." Bayer (2003):
- "Product Information. Cialis (tadalafil)." Lilly, Eli and Company (2003):
- "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group (2005):
- "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation (2009):
- "Product Information. Stendra (avanafil)." Vivus Inc (2012):
- "Product Information. Staxyn (vardenafil)." Merck & Co., Inc (2014):
Therapeutic duplication
Drug classes that overlap with Avanafil, so taking both doubles up the same effect. This source publishes no per-row citations for duplication.
erectile dysfunction agents
The recommended maximum number of medicines in the 'erectile dysfunction agents' category to be taken concurrently is usually one.Your list includes two medicines belonging to the 'erectile dysfunction agents' category.
Example product in the source data (US market): Finasteride/tadalafil