20 Mg Vardenafil

Other > vardenafil 5 mg


The maximum decrease in blood pressure occurred

Aspect Description Typical Dosage Onset Time Duration of Action
Vardenafil 5 mg A medication used to treat erectile dysfunction 5 mg 30-60 min Up to 4-5 hours
Pharmacological Class Phosphodiesterase type 5 inhibitor N/A N/A N/A
Brand Names Levitra, Staxyn (dissolvable film) N/A N/A N/A

between 1 and 4 hours after dosing.

Product Description

This protein binding is reversible and independent of total drug concentrations. Following a single oral dose of 20 mg vardenafil in healthy volunteers, a mean of 0.00018% of the administered dose was obtained in semen 1.5 hours after dosing. Vardenafil is metabolized predominantly by the hepatic enzyme CYP3A4, with contribution from the CYP3A5 and CYP2C isoforms. The major circulating metabolite, M1, results from desethylation at the piperazine moiety of vardenafil. The plasma concentration of M1 is approximately 26% that of the parent compound.

More common

This metabolite shows a phosphodiesterase selectivity profile similar to that of vardenafil and an in vitro inhibitory potency for PDE5 28% of that of vardenafil. Therefore, M1 accounts for approximately 7% of total pharmacologic activity. The total body clearance of vardenafil is 56 L/h, and the terminal half-life of vardenafil and its primary metabolite (M1) is approximately 4-5 hours. After oral administration, vardenafil is excreted as metabolites predominantly in the feces (approximately 91-95% of administered oral dose) and to a lesser extent in the urine (approximately 2-6% of administered oral dose). Pediatrics: Vardenafil trials were not conducted in the pediatric population.

Visual disturbances

Geriatrics: In a healthy volunteer study of elderly males (≥65 years) and younger males (18–45 years), mean Cmax and AUC were 34% and 52% higher, respectively, in the elderly males (see PRECAUTIONS, Geriatric Use and DOSAGE AND ADMINISTRATION). Consequently, a lower starting dose of LEVITRA (5 mg) in patients ≥65 years of age should be considered. Renal Insufficiency: In volunteers with mild renal impairment (CLcr = 50-80 ml/min), the pharmacokinetics of vardenafil were similar to those observed in a control group with normal renal function. In the moderate (CLcr = 30-50 ml/min) or severe (CLcr<30 ml/min) renal impairment groups, the AUC of vardenafil was 20–30% higher compared to that observed in a control group with normal renal function (CLcr>80 ml/min). Vardenafil pharmacokinetics have not been evaluated in patients requiring renal dialysis (see PRECAUTIONS, Renal Insufficiency, and DOSAGE AND ADMINISTRATION). Following multiple dosing for

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31 days, similar blood pressure

Side Effect Frequency Severity Management Tips
Headache Common Mild to Moderate Hydration, OTC pain relief
Flushing Frequently reported Mild Cool environment, calming techniques
Nasal congestion Sometimes Mild Decongestants (if advised)
Dizziness Occasionally Mild Sit or lie down, avoid driving
Upset stomach Less common Mild Take with food, monitor symptoms

responses were observed on Day 31 as on Day 1.