Pharmacokinetics
The pharmacokinetic profile of Vardenafil 20mg elucidates its absorption, distribution, metabolism, and excretion. Upon oral administration, Vardenafil is rapidly absorbed. Peak plasma concentrations appear within one hour. The absolute bioavailability hovers around 15%. This figure underscores the substantial first-pass metabolism characteristic of this phosphodiesterase type 5 (PDE5) inhibitor.
Vardenafil’s volume of distribution is approximately 208 L, indicating extensive tissue distribution. Protein binding is notable at about 95%. This high degree of protein affinity implies minimal free drug available in the plasma, impacting its efficacy and duration of action. Vardenafil is extensively metabolized, primarily by hepatic enzymes CYP3A4, with contributions from CYP3A5 and CYP2C isoforms.
The half-life of Vardenafil is around 4-5 hours. This duration facilitates a therapeutic window sufficient for its intended use while limiting prolonged exposure. Excretion occurs predominantly via fecal pathways (91-95%) with renal pathways accounting for a smaller fraction.
Mechanism of Action
Vardenafil 20mg operates by selectively inhibiting PDE5, an enzyme responsible for cGMP degradation in the corpus cavernosum. Inhibition of PDE5 leads to increased levels of cGMP. Elevated cGMP results in smooth muscle relaxation, engorgement of blood in penile tissues, and, ultimately, erection.
The effectiveness of Vardenafil is contingent on sexual stimulation. Neural nitric oxide (NO) release catalyzes the conversion of GTP to cGMP by guanylate cyclase. Vardenafil potentiates this NO-mediated process, amplifying its therapeutic effect in erectile dysfunction (ED).
FDA-Approved Indications
The FDA endorses Vardenafil 20mg for treating erectile dysfunction. Its primary clinical utility centers on enabling males with ED to achieve and maintain satisfactory erections. The medication is prescribed following a thorough assessment of cardiovascular status.
While indicated for ED, Vardenafil is contraindicated with nitrate medications due to potential hypotensive crises. The clinical trials leading to approval highlighted its favorable efficacy and tolerability profile in the male population.
Vardenafil Interactions
Interaction profiles of Vardenafil 20mg necessitate caution. Co-administration with potent CYP3A4 inhibitors such as ketoconazole, ritonavir, or indinavir results in elevated plasma levels of Vardenafil, increasing adverse effects.
Nitrates and alpha-blockers present a risk of severe hypotension when used with Vardenafil. Alcohol consumption may amplify hypotensive effects. Awareness of potential interactions assists clinicians in preventing complications.
Toxicity
Toxicity concerns with Vardenafil 20mg include cardiovascular risks, particularly in patients with underlying heart conditions. Overdose may precipitate symptoms such as severe back pain, blurred vision, or syncope. Immediate medical intervention is advised if these occur.
Post-marketing surveillance has not indicated significant new safety signals. However, clinicians should be vigilant for priapism, a rare but serious adverse reaction necessitating urgent care.
Where to buy Vardenafil online
Vardenafil 20mg is accessible via various online pharmaceutical retailers. It is imperative to purchase from licensed pharmacies to ensure drug authenticity and safety. For comprehensive pharmaceutical information, reference this source.
Adherence to recommended dosages and consideration of the potential for drug interactions enhance therapeutic outcomes. Verify online platforms for credentials and legitimacy before procuring Vardenafil.
Property | Vardenafil 20mg |
---|---|
Bioavailability | ~15% |
Half-Life | 4-5 hours |
Protein Binding | 95% |
Excretion | 91-95% fecal |