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Do not chew, crush or break it. Counseling of patients about protective measures necessary to guard against sexually transmitted diseases, including the Human Immunodeficiency Virus (HIV), should be considered.The following serious adverse reactions with the use of Levitra (vardenafil) are discussed elsewhere in the labeling:Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.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. 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).Levitra is not indicated for use in pediatric patients.
Levitra may be taken with or without meals.Do not change your dose of Levitra without talking to your doctor. Swallow it as a whole. Therefore, the use of such combinations is not recommended.In humans, vardenafil alone in doses up to 20 mg does not prolong the bleeding time. No evidence of specific potential for teratogenicity, embryotoxicity or fetotoxicity was observed in rats and rabbits that received vardenafil at up to 18 mg/kg/day during organogenesis. The maximum dose of Levitra for which human data are available is a single 120 mg dose administered to healthy male volunteers. It is not possible to determine whether these events are related directly to the PDE5 inhibitors, to other diseases or medications, to other factors, or to a combination of factors. quinidine, procainamide) or Class III (for example, amiodarone, sotalol) antiarrhythmic medications or those with congenital QT prolongation, should avoid using Levitra.Dosage adjustment is necessary in patients with moderate hepatic impairment (Child-Pugh B). There was significant improvement (p <0.0001) at 3 months with Levitra (EF Domain scores of 18, 21, 21, for the 5 mg, 10 mg, and 20 mg dose groups, respectively) compared to the placebo group (EF Domain score of 15).

You and your doctor should talk about Levitra when you start taking it and at regular checkups. Levitra should be taken approximately 60 minutes before sexual activity. Counsel patients that protective measures necessary to guard against sexually transmitted diseases, including the Human Immunodeficiency Virus (HIV), should be considered.Inform patients that the recommended starting dose of Levitra is 10 mg. Weak inhibitory effects toward other isoforms (CYP2C8, 2C9, 2C19, 2D6, 3A4) were found, but Ki values were in excess of plasma concentrations achieved following dosing. Signs of low mood (depression), thoughts of killing yourself, nervousness, emotional ups and downs, thinking that is not normal, anxiety, or lack of interest in life. Vardenafil HCl is a nearly colorless, solid substance with a molecular weight of 579.1 g/mol and a solubility of 0.11 mg/mL in water. )Figure 1: Placebo-subtracted point estimates (with 90% CI) of mean maximal blood pressure and heart rate effects of pre-dosing with vardenafil 20 mg at 24, 8, 4, and 1 hour before 0.4 mg NTG sublinguallyBecause the disease state of patients requiring nitrate therapy is anticipated to increase the likelihood of hypotension, the use of vardenafil by patients on nitrate therapy or on nitric oxide donors is contraindicated Three clinical pharmacology studies were conducted in patients with benign prostatic hyperplasia (BPH) on stable-dose alpha-blocker treatment, consisting of alfuzosin, tamsulosin or terazosin.Blood pressure effects (standing SBP) in normotensive men on stable dose of tamsulosin 0.4 mg following simultaneous administration of vardenafil 5 mg or placebo, or following administration of vardenafil 5 mg or placebo separated by 6 hours are shown in Figure 2. No muscle or neurological toxicity was identified.In cases of overdose, standard supportive measures should be taken as required. Levitra 30mg - A month's worth of pills is available from wholesalers for less than $20. It works by attaching to specific sites (SV2A) on the surfaces of nerve cells. Levitra is not for women or children.

Do not change the dose or stop this drug. Levitra (vardenafil) is a prescription medication used to treat impotence (or erectile dysfunction, ED, the inability to attain or maintain a penile erection). If you are not sure what to do, you can contact your doctor.Levitra 500mg Tablet may take a few weeks to start working properly since the dose is increased slowly. Please consult your doctor.Levitra 500mg Tablet is probably safe to use in patients with liver disease. Levitra 500mg Tablet is an anti-epileptic medicine used to treat seizures (fits) in epilepsy. If priapism is not treated immediately, penile tissue damage and permanent loss of potency may result.Levitra should be used with caution by patients with anatomical deformation of the penis (such as angulation, cavernosal fibrosis, or Peyronie’s disease) or by patients who have conditions that may predispose them to priapism (such as sickle cell anemia, multiple myeloma, or leukemia).Physicians should advise patients to stop use of all phosphodiesterase type 5 (PDE5) inhibitors, including Levitra, and seek medical attention in the event of sudden loss of vision in one or both eyes.
Once a man has completed sexual activity, blood flow to his penis decreases, and his erection goes away.Talk to your doctor to decide if Levitra is right for you.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.Take 1 Levitra tablet about 1 hour (60 minutes) before sexual activity. You can gain your confidence and sex power by life style modification. The mean baseline EF Domain scores were 13, 13, 13, 14 for the Levitra 5 mg, 10 mg, 20 mg and placebo groups, respectively. Individuals who have already experienced NAION are at increased risk of NAION recurrence.
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