Adult: As conventional tab: Usual dose: 10 mg as needed; may adjust according to response (range: 5-20 mg). As orodispersible tab: Max: 10 mg as needed. Dose is taken approx 25-60 minutes before sexual intercourse. Max dosing frequency: Once every 24 hours. Elderly: As conventional tab: 5 mg as needed, at least 25-60 minutes before sexual intercourse. Max: 20 mg. Max dosing frequency: Once every 24 hours.
Special Patient Group
Patients taking α-blockers: As conventional tab: Max: 5 mg daily. As orodispersible tab: Co-administer within a 6 hour-interval.
Patient taking CYP3A4 inhibitors: As conventional tab: 2.5 mg once every 24 hours with ketoconazole 400 mg, itraconazole 400 mg, clarithromycin; 2.5 mg once every 72 hours with ritonavir; 5 mg once every 24 hours with erythromycin, ketoconazole 200 mg, itraconazole 200 mg.
Patient taking HIV-protease inhibitors: As conventional tab: 2.5 mg once every 24 hours.
As conventional tab:
Initially, 5 mg as needed, at least 25-60 minutes before sexual intercourse. Dose may be increased to 10-20 mg according
Mild to moderate (Child-Pugh class A or B) As conventional tab: Initially, 5 mg as needed, at least 25-60 minutes before sexual intercourse. Max: 10 mg. Max dosing frequency: Once every 24 hours. Severe (Child-Pugh class C): Contraindicated.
May be taken with or without food.
Chống chỉ định
Severe CV disorder or recent history of stroke or MI (within the last 6 months), unstable angina, retinitis pigmentosa, vision loss due to non-arteritic anterior ischaemic optic neuropathy (NAION), ESRD requiring dialysis, hypotension <90/50 mmHg, and other conditions wherein sexual intercourse is inadvisable. Severe hepatic impairment (Child-Pugh class C). Concomitant use with any form of organic nitrates/nitrites, guanylate cyclase stimulators
Patient with CV disease, left ventricular outflow obstruction (aortic stenosis or hypertrophic obstructive cardiomyopathy), anatomical penile deformation, conditions which may predispose to priapism (e.g. sickle cell anaemia, multiple myeloma, leukaemia); bleeding disorders, peptic ulcer disease. Severe renal and mild to moderate hepatic impairment. Elderly. Pregnancy and lactation.
Phản ứng phụ
Significant: Hypotension, color discrimination impairment, vision loss/NAION, sudden decrease or loss of hearing, tinnitus. Rarely, prolonged/painful erection or priapism. Gastrointestinal disorders: Dyspepsia, nausea. General disorders and administration site conditions: Flu-like symptoms. Nervous system disorders: Headache, dizziness. Respiratory, thoracic and mediastinal disorders: Nasal congestion, sinusitis.
This medicine may cause dizziness and blurred vision, if affected, do not drive or operate machinery.
Assess CV status prior to initiation of therapy. Monitor BP, heart rate, renal function, and LFT.
Symptoms: Back pain/myalgia, abnormal vision. Management: Supportive treatment.
May enhance hypotensive effect of α-blockers. Increased serum concentration with guanylate cyclase stimulators (e.g. riociguat), potent CYP3A4 inhibitors (e.g. ketoconazole) and moderate CYP3A4 inhibitors (e.g. clarithromycin), HIV protease inhibitors (e.g. ritonavir). May prolong Qt interval with class IA (e.g. quinidine, procainamide) or class III (e.g. amiodarone, sotalol) antiarrhythmics. Potentially Fatal: Enhanced hypotensive effect with any form of organic nitrates/nitrites, guanylate cyclase stimulators (e.g. riociguat).
Increased serum concentration with grapefruit juice.
Description: Vardenafil is a potent phosphodiesterase inhibitor with the greatest selectivity for PDE type 5, which is responsible for the metabolism of cyclic guanosine monophosphate (cGMP) in the smooth muscle. Inhibition of PDE type 5 causes smooth muscle relaxation and increased blood flow into the corpus cavernosum of the penis during sexual stimulation, thereby producing an erection. Onset: Approx 60 minutes. Pharmacokinetics: Absorption: Rapidly absorbed from the gastrointestinal tract. Food, particularly high-fat meal, decreases rate of absorption. Bioavailability: Approx 15%. Time to peak plasma concentration: 0.5-2 hours. Distribution: Widely distributed in the tissues. Volume of distribution: 208 L. Detected in the semen. Plasma protein binding: Approx 95% (parent drug and metabolite). Metabolism: Metabolised in the liver primarily by CYP3A4 as well as CYP3A5 and CYP2C via desethylation into active metabolite. Excretion: Mainly via faeces (approx 91-95%, as metabolites); urine (approx 2-6%). Terminal half-life: Approx 4-6 hours.
G04BE09 - vardenafil ; Belongs to the class of drugs used in erectile dysfunction.
Anon. Vardenafil. Lexicomp Online. Hudson, Ohio. Wolters Kluwer Clinical Drug Information, Inc. https://online.lexi.com. Accessed 12/01/2018.Buckingham R (ed). Vardenafil. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 12/01/2018.Joint Formulary Committee. Vardenafil. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 12/01/2018.Levitra Film Coated Tablet (GlaxoSmithKline LLC). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/. Accessed 12/01/2018.