FDA label 7d55d7b6-4e8d-2691-e053-2a91aa0a77b6
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- SPL set ID
- f18a82f7-ce44-4f9c-ae69-d3ad1d375564
- SPL ID
- 7d55d7b6-4e8d-2691-e053-2a91aa0a77b6
- Version
- 3
- Effective date
- 2018-12-18
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:20:11
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | 7d55d7b6-4e8d-2691-e053-2a91aa0a77b6 | id | |
| spl set id | f18a82f7-ce44-4f9c-ae69-d3ad1d375564 | set_id |
Warnings cross-check#
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WARNINGS Cardiovascular effects General: Physicians should consider the cardiovascular status of their patients, since there is a degree of cardiac risk associated with sexual activity. In men for whom sexual activity is not recommended because of their underlying cardiovascular status, any treatment for erectile dysfunction, including LEVITRA, generally should not be used. Left Ventricular Outflow Obstruction: Patients with left ventricular outflow obstruction, e.g., aortic stenosis and idiopathic hypertrophic subaortic stenosis, can be sensitive to the action of vasodilators including Type 5 phosphodiesterase inhibitors. Blood Pressure Effects: LEVITRA has systemic vasodilatory properties that resulted in transient decreases in supine blood pressure in healthy volunteers (mean maximum decrease of 7 mmHg systolic and 8 mmHg diastolic) (see CLINICAL PHARMACOLOGY , Pharmacodynamics ). While this normally would be expected to be of little consequence in most patients, prior to prescribing LEVITRA, physicians should carefully consider whether their patients with underlying cardiovascular disease could be affected adversely by such vasodilatory effects. Effect of Co-administration of Potent CYP3A4 Inhibitors Long-term safety information is not available on the concomitant administration of vardenafil with HIV protease inhibitors. Concomitant administration with ritonavir or indinavir substantially increases plasma concentrations of vardenafil. Because ritonavir prolongs LEVITRA elimination half-life (5 to 6-fold), no more than a single 2.5 mg dose of LEVITRA should be taken in a 72-hour period by patients also taking ritonavir. Patients taking indinavir, saquinavir, atazanavir or other potent CYP3A4 inhibitors such as clarithromycin, ketoconazole 400 mg daily, or itraconazole 400 mg daily should not exceed a dose of LEVITRA 2.5 mg once daily. For patients taking ketoconazole 200 mg daily or itraconazole 200 mg daily, a single dose of 5 mg LEVITRA should not be exceeded in a 24-hour period (see PRECAUTIONS , Drug Interactions and DOSAGE AND ADMINISTRATION ). Other Effects There have been rare reports of prolonged erections greater than 4 hours and priapism (painful erections greater than 6 hours in duration) for this class of compounds, including vardenafil. In the event that an erection persists longer than 4 hours, the patient should seek immediate medical assistance. If priapism is not treated immediately, penile tissue damage and permanent loss of potency may result. Patient Subgroups Not Studied in Clinical Trials There are no controlled clinical data on the safety or efficacy of LEVITRA in the following patients; and therefore its use is not recommended until further information is available. unstable angina; hypotension (resting systolic blood pressure of <90 mmHg); uncontrolled hypertension (>170/110 mmHg); recent history of stroke, life-threatening arrhythmia, or myocardial infarction (within the last 6 months); severe cardiac failure severe hepatic impairment (Child-Pugh C) end stage renal disease requiring dialysis known hereditary degenerative retinal disorders, including retinitis pigmentosa
Adverse reactions cross-check#
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adverse reactions
ADVERSE REACTIONS LEVITRA was administered to over 4430 men (mean age 56, range 18-89 years; 81% White, 6% Black, 2% Asian, 2% Hispanic and 9% Other) during controlled and uncontrolled clinical trials worldwide. Over 2200 patients were treated for 6 months or longer, and 880 patients were treated for at least 1 year. In placebo-controlled clinical trials, the discontinuation rate due to adverse events was 3.4% for LEVITRA compared to 1.1% for placebo. When LEVITRA was taken as recommended in placebo-controlled clinical trials, the following adverse events were reported (see Table 5 ). Table 5: Adverse Events Reported By ≥2% of Patients Treated with LEVITRA and More Frequent on Drug than Placebo in Fixed and Flexible Flexible dose studies started all patients at LEVITRA 10 mg and allowed decrease in dose to 5 mg or increase in dose to 20 mg based on side effects and efficacy. Dose Randomized, Controlled Trials of 5 mg, 10 mg, or 20 mg Vardenafil Adverse Event Percentage of Patients Reporting Event Placebo N = 1199 LEVITRA N = 2203 Headache 4% 15% Flushing 1% 11% Rhinitis 3% 9% Dyspepsia 1% 4% Accidental Injury All the events listed in the above table were deemed to be adverse drug reactions with the exception of accidental injury. 2% 3% Sinusitis 1% 3% Flu Syndrome 2% 3% Dizziness 1% 2% Increased Creatine Kinase 1% 2% Nausea 1% 2% Back pain was reported in 2.0% of patients treated with LEVITRA and 1.7% of patients on placebo. Placebo-controlled trials suggested a dose effect in the incidence of some adverse events (headache, flushing, dyspepsia, nausea, rhinitis) over the 5 mg, 10 mg, and 20 mg doses of LEVITRA. The following section identifies additional, less frequent events (<2%) reported during the clinical development of LEVITRA. Excluded from this list are those events that are infrequent and minor, those events that may be commonly observed in the absence of drug therapy, and those events that are not reasonably associated with the drug. BODY AS A WHOLE: anaphylactic reaction (including laryngeal edema), asthenia, face edema, pain AUDITORY: sudden decrease or loss of hearing, tinnitus CARDIOVASCULAR: angina pectoris, chest pain, hypertension, hypotension, myocardial ischemia, myocardial infarction, palpitation, postural hypotension, syncope, tachycardia DIGESTIVE: abdominal pain, abnormal liver function tests, diarrhea, dry mouth, dysphagia, esophagitis, gastritis, gastroesophageal reflux, GGTP increased, vomiting MUSCULOSKELETAL: arthralgia, back pain, myalgia, neck pain NERVOUS: hypertonia, hypesthesia, insomnia, paresthesia, somnolence, vertigo RESPIRATORY: dyspnea, epistaxis, pharyngitis SKIN AND APPENDAGES: photosensitivity reaction, pruritus, rash, sweating OPHTHALMOLOGIC: abnormal vision, blurred vision, chromatopsia, changes in color vision, conjunctivitis (increased redness of the eye), dim vision, eye pain, glaucoma, photophobia, watery eyes UROGENITAL: abnormal ejaculation, priapism (including prolonged or painful erections)
adverse reactions table
<table width="0.000" ID="id_ea3448df-5240-4566-be8b-220aea37874a"> <caption ID="id_cfdabc4a-a187-4124-828d-127390a90402">Table 5: Adverse Events Reported By ≥2% of Patients Treated with LEVITRA and More Frequent on Drug than Placebo in Fixed and Flexible <footnote ID="id-c2c2f144-ba76-45c3-87b3-55e95a284adf">Flexible dose studies started all patients at LEVITRA 10 mg and allowed decrease in dose to 5 mg or increase in dose to 20 mg based on side effects and efficacy.</footnote> Dose Randomized, Controlled Trials of 5 mg, 10 mg, or 20 mg Vardenafil </caption> <col/> <col/> <col/> <thead> <tr ID="id_b644e820-225d-4899-a677-fc575d07780b"> <td align="center" styleCode="Toprule" valign="top">Adverse Event</td> <td align="left" colspan="2" valign="top">Percentage of Patients Reporting Event</td> </tr> <tr ID="id_fa38e584-1d64-4704-a5ec-171f1a1b1d87"> <td align="left" styleCode="Botrule" valign="top"/> <td align="left" styleCode="Botrule" valign="top">Placebo N = 1199 </td> <td align="left" styleCode="Botrule" valign="top">LEVITRA N = 2203 </td> </tr> </thead> <tbody> <tr ID="id_b4cff050-48bc-454f-843e-60dcb36aa4de"> <td align="left" styleCode="Toprule" valign="top">Headache</td> <td align="left" styleCode="Toprule" valign="top">4%</td> <td align="left" valign="top">15%</td> </tr> <tr ID="id_ad6a0d2f-11c2-46e3-8621-73db6e15decb"> <td align="left" valign="top">Flushing</td> <td align="left" valign="top">1%</td> <td align="left" valign="top">11%</td> </tr> <tr ID="id_5801e014-c1d9-4fb8-bd92-87a7e15e7908"> <td align="left" valign="top">Rhinitis</td> <td align="left" valign="top">3%</td> <td align="left" valign="top">9%</td> </tr> <tr ID="id_44a3110f-4b06-44d0-9013-69a2d53a8f1b"> <td align="left" valign="top">Dyspepsia</td> <td align="left" valign="top">1%</td> <td align="left" valign="top">4%</td> </tr> <tr ID="id_93a051cf-126b-4240-a208-b00c0bb4a6d4"> <td align="left" valign="top">Accidental Injury <footnote ID="id-c61c65c2-8ed4-47e2-870b-22bf42eea9d7">All the events listed in the above table were deemed to be adverse drug reactions with the exception of accidental injury. </footnote> </td> <td align="left" valign="top">2%</td> <td align="left" valign="top">3%</td> </tr> <tr ID="id_5a230d84-27c7-456a-9589-00d33713d961"> <td align="left" valign="top">Sinusitis</td> <td align="left" valign="top">1%</td> <td align="left" valign="top">3%</td> </tr> <tr ID="id_46ce0fdb-54f0-4353-aee3-4ae4aebd8f33"> <td align="left" valign="top">Flu Syndrome</td> <td align="left" valign="top">2%</td> <td align="left" valign="top">3%</td> </tr> <tr ID="id_80e91f73-81c0-4b84-86ba-a76e689f621e"> <td align="left" valign="top">Dizziness</td> <td align="left" valign="top">1%</td> <td align="left" valign="top">2%</td> </tr> <tr ID="id_19b06819-22fa-48b0-b55f-5410cd071966"> <td align="left" valign="top">Increased Creatine Kinase</td> <td align="left" valign="top">1%</td> <td align="left" valign="top">2%</td> </tr> <tr ID="id_921af732-3fee-4dad-b3a8-7068a117a297"> <td align="left" styleCode="Botrule" valign="top">Nausea</td> <td align="left" styleCode="Botrule" valign="top">1%</td> <td align="left" styleCode="Botrule" valign="top">2%</td> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.