Vardenafil is a medication that treats erectile dysfunction. ED is the inability to achieve and sustain an erection suitable for sexual intercourse. This medication works by increasing blood flow to your penis, which helps you maintain an erection. LEVITRA was administered to over 4430 men (mean age 56, range years; 81% White, 6% Black, online xanax store 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.
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Consequently, it is recommended not to exceed a single 2.5 mg LEVITRA dose in a 72-hour period when used in combination with ritonavir. [see DOSAGE AND ADMINISTRATION and WARNINGS AND PRECAUTIONS]. In the placebo-controlled clinical trials for LEVITRA film-coated tablets and vardenafil orally disintegrating tablets, the discontinuation rate due to adverse events was 1.9% for vardenafil compared to 0.8% for placebo.
LEVITRA has not been evaluated in patients with known hereditary degenerative retinal disorders, including retinitis pigmentosa, therefore its use is not recommended until further information is available in those patients. The evaluation of erectile dysfunction should include a medical assessment, a determination of potential underlying causes and the identification of appropriate treatment. The following adverse reactions have been identified during post approval use of LEVITRA. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency or establish a causal relationship to drug exposure.
The safety and efficacy of LEVITRA used in combination with other treatments for erectile dysfunction have not been studied. Although specific interactions have not been studied, other CYP3A4 inhibitors, including grapefruit juice would likely increase vardenafil exposure. Back pain was reported in 2.0% of patients treated with LEVITRA and 1.7% of patients on placebo. A time interval between dosing should be considered when Levitra is prescribed concomitantly with alpha-blocker therapy [see CLINICAL PHARMACOLOGY].
This drug does not protect against sexually transmitted diseases (such as HIV, hepatitis B, gonorrhea, syphilis). This means that a licensed health care provider must authorize the use of this medication. Do not exceed the dosage prescribed or discontinue using Levitra without consulting your health care provider first.
Advise patients to contact the prescribing physician if new medications that may interact with LEVITRA are prescribed by another healthcare provider. Inform patients that LEVITRA is contraindicated with regular and/or intermittent use of organic nitrates. In humans, vardenafil alone in doses up to 20 mg does not prolong the bleeding time.
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Levitra has been shown to be effective in men over the age of 18 years who have erectile dysfunction, including men with diabetes or who have undergone prostatectomy. Levitra is not covered under Part D of Medicare, an optional Medicare benefit that can help cover the costs of eligible prescription medications. RxSaver is a prescription medication savings company that offers coupons for a variety of medications, including Levitra. While Levitra is usually prescribed in doses of 10 to 20 mg, generic vardenafil may be sold in tablets as small as 2.5 mg up to 20 mg. The above information is intended to supplement, not substitute for, the expertise and judgment of your health care professional. You should consult your health care professional before taking any drug, changing your diet, or commencing or discontinuing any course of treatment.
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Concomitant treatment with vardenafil and alpha-blockers should be initiated only if the patient is stable on his alpha-blocker therapy. In those patients who are stable on alpha-blocker therapy, LEVITRA should be initiated at the lowest recommended starting dose (see DOSAGE and ADMINISTRATION). The most common side effects of vardenafil are listed below. These side effects may vary depending on the form of vardenafil prescribed. Tell your healthcare provider if you have any of these side effects that bother you.
Individuals who have already experienced NAION are at increased risk of NAION recurrence. Therefore, PDE5 inhibitors, including LEVITRA, should be used with caution in these patients and only when the anticipated benefits outweigh the risks. Alcohol and vardenafil plasma levels were not altered when dosed simultaneously. When LEVITRA was taken as recommended in placebo-controlled clinical trials, the following adverse reactions were reported (see Table 1). In placebo-controlled clinical trials, the discontinuation rate due to adverse events was 3.4% for LEVITRA compared to 1.1% for placebo. LEVITRA (vardenafil hydrochloride) is administered orally for the treatment of erectile dysfunction.