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Avana (Avanafil)
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Avana

Avana is used to treat male sexual function problems (impotence or erectile dysfunction - ED). In combination with sexual stimulation, Avana works by increasing blood flow to the penis to help a man get and keep an erection. This drug does not protect against sexually transmitted diseases (such as HIV, hepatitis B, gonorrhea, syphilis).

Other names for this medication:
Avanafil, Spedra, Stendra

Similar Products:
Ceclor, Flomax, Astelin, Minocin, Cozaar, Trandate, Etyphyllin, Soma, Melacare, Alvergy, Agemax, Lemohist, Propra, Erazol, Histagra,

Also known as: Avanafil

Description

Avana is FDA-approved anti-impotence drug manufactured by Sunrise Remedies. The active ingredient of Avana is Avanafil, which is classified as PDE5 inhibitor and is aimed to treat male sexual dysfunction. Other well-known agents share a similar mechanism of action as Avanafil: Tadalafil (Cialis), Sildenafil (Viagra) and Vardenafil (Levitra). Once a drug is absorbed into the bloodstream, Avanafil expands muscles in the walls of blood vessels, thereby increases blood flow into the penis and provides a strong erection. The effect of medication starts in 15-30 minutes after taking and can last up to 6 hours, allowing you to choose the most appropriate time for you and your partner. Avanafil helps to achieve an erection when sexual stimulation occurs. Avana doesn't protect you and your partner from sexually transmitted diseases (including HIV) and from pregnancy. Avana is not intended for the treatment in women and children.

Dosage

Take one pill orally with a full glass of water 15-30 minutes before sexual activity. It may be taken with or without food. Start with 50 mg, if you are undergoing stable alpha-blocker therapy or have other health issues. You should not take the medication more than once a day or more than a recommended dose.

Overdose

If an overdose occurs and you are not feeling well, you should seek emergency medical attention or contact your healthcare provider immediately.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) and away from excess moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Avana are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Avana if you are allergic to Avana's components. Do not take Avana if you are also using organic nitrates, nitrate drug for chest pain or heart condition (e.g., nitroglycerin, isosorbide dinitrate, and isosorbide mononitrate), nitrates as amyl nitrate or nitrite ("poppers"). Do not take Avana if you take other medication to treat erectile dysfunction, pulmonary arterial hypertension, such as riociguat (Adempas). Do not take Avana in case you are taking erythromycin, medicines called alpha-blockers, ketoconazole, itraconazole (Sporanox or Nizoral), ritonavir (Norvir) or indinavir (Crixivan). Try not to consume alcohol while using Avana, as it can lower your blood pressure, causing dizziness and rapid heart rate (tachycardia). Do not drive or operate machinery while taking the medication. Contact you doctor or health care professional right away if the erection lasts longer than 4 hours or if it becomes painful. Avana does not protect you and your partner from sexually transmitted diseases and pregnancy. Avana can be dangerous for children and women.

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The epitopes encompassed within the CNBr2 portion of pili appear to be inaccessible to anti-CNBr2 probes within native gonococcal pili. Synthetic oligonucleotides (oligomers) complementary to vesicular stomatitis virus (VSV) N protein mRNA have specific antiviral properties at concentrations lower than 1 microM when they are covalently linked to poly(L-lysine) (PLL). A review of literature on medical students and scholarly research: experiences, attitudes, and outcomes. Phylogenetic analyses revealed orthologs of OsJAC1 exclusively within the Poaceae plant family. This study focused on two main points: (1) determining the prevalence of R5 and X4 HIV strains in antiretroviral-experienced patients using two main tests currently in use to determine viral tropism, and (2) the follow-up to 3 years of a limited number of patients who started a new antiretroviral protocol including maraviroc. To determine the reason for increased pulmonary distensibility in excised lungs, we performed deflation pressure-volume (PV) studies in 24 dogs. In this study we aimed to develop the Japanese version of CLDQ and to assess its validity and reliability in Japanese patients with chronic viral hepatitis. For both cohorts relative risks of 1.2-1.4 were found for the 5-year period immediately following diagnosis, likely resulting from the uncontrolled effect of stage in the analysis.

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Illness representations of depression (IPQ-R) and perceptions of the helpfulness of different social support behaviors (ISU-DYA and ISAD) were assessed in 41 currently depressed persons colospa x dose and 58 persons without a history of depression. The scale of demographic heterogeneity in a population of Peromyscus leucopus. These changes in endothelium function may promote vasospasm and vascular occlusion and contribute to increased vascular resistance in hypertension. Navigated retinal laser photocoagulation demonstrated safety and accuracy for the treatment of acute CSC. Public support for smoke-free policies in Jordan, a high tobacco burden country with weak implementation of policies: Status, opportunities, and challenges. Patients with peripheral arterial disease (PAD) have high rates of adverse cardiovascular events after percutaneous coronary intervention and may additionally have heightened platelet reactivity. Additionally, we examined the involvement of ROS generation in the effect of TBBPA. We report a case of metastatic bladder tumor from gastric cancer, which was difficult to differentiate from urachal tumor preoperatively, especially computed tomographic scan, cystoscopy, and biopsy. In vitro, however, amylase secretion was not affected by the peptide: it had no affect either on basal secretion, or on stimulated secretion induced via CCK-, or cholinergic receptors. This study, and others with similar results, suggests that our view of the chromosomal evolution of the house mouse should be revised.

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