Avanafil (Stendra)

Avanafil (Stendra) FDA Approval History

April 27, 2012 - The U.S. Food and Drug Administration today endorsed Stendra (avanafil), another medication to treat erectile brokenness. Erectile brokenness is the point at which a man experiences difficulty getting or keeping an erection. An expected 30 million men in the United States are influenced by erectile brokenness. Stendra is a pill that patients take dependent upon the

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Avanafil (Stendra)

Avanafil (Stendra): Drug Class (Impotence Agents)

STENDRA (avanafil) is a particular inhibitor of cGMP-explicit PDE5.  Avanafil is assigned artificially as (S)- 4- [(3-Chloro-4-methoxybenzyl) amino] -2- [2-(hydroxymethyl)- 1-pyrrolidinyl]-N (2-pyrimidinylmethyl)- 5-pyrimidinecarboxamide  Avanafil happens as white translucent powder, atomic equation C23H26ClN7O3 and sub-atomic load of 483.95 and is marginally dissolvable in ethanol, for all intents and purposes insoluble in water, solvent in 0.1 mol/L hydrochloric corrosive. STENDRA, for oral

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Avanafil (Stendra)

Avanafil (Stendra): Generic Availability

There is right now no remedially identical variant of Stendra accessible in the United States. Note: Fraudulent online drug stores may endeavor to sell an unlawful conventional adaptation of Stendra. These drugs might be fake and conceivably hazardous. On the off chance that you buy meds on the web, be certain you are purchasing from a respectable and legitimate online

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Avanafil (Stendra)

Avanafil (Stendra): Drug Interactions

Potential For Pharmacodynamic Interactions With Stendra Nitrates Organization of Stendra to patients who are utilizing any type of natural nitrate, is contraindicated. In a clinical pharmacology preliminary, Stendra was displayed to potentiate the hypotensive impact of nitrates. In a taken patient Stendra, where nitrate organization is considered restoratively significant in a perilous circumstance, somewhere around 12 hours ought to slip

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Avanafil (Stendra)

Avanafil (Stendra): Patient Tips

Assessment of erectile dysfunction(ED) ought to incorporate a suitable clinical appraisal to distinguish possible fundamental causes, just as treatment choices. Prior to endorsing Avanafil (Stendra), note the accompanying: There is a potential for heart hazard during sexual movement in patients with prior cardiovascular illness. Consequently, medicines for ED, including Avanafil (Stendra), ought not be utilized in men for whom sexual

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Avanafil (Stendra)

Avanafil (Stendra): Dosage Information

For most people, the suggested beginning portion of avanafil is 100 mg each day required around 30 minutes before sexual action. Contingent upon the sufficiency of the reaction or incidental effects, the portion might be expanded to 200 mg or diminished to 50 mg daily. People who are taking meds that decently increment the blood levels of avanafil ought not

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Avanafil (Stendra)

Avanafil (Stendra): During Pregnancy

Animal experimentations have uncovered decreased posterity development. There is no sure information about human pregnancy.  US FDA pregnancy classification Not Assigned: The US FDA has altered the pregnancy naming standard for physician endorsed drug items to require marking that incorporates an outline of hazard, a conversation of the information supporting that synopsis, and applicable data to help medical services suppliers

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Vardenafil (Levitra)

Vardenafil (Levitra): FDA Approval History

FDA endorsement of Levitra depended on four multi-focus, twofold visually impaired, randomized, fake treatment controlled, fixed-portion, equal plan preliminaries. The examinations selected an aggregate of 2431 men with a normal age of 57 years. The dosages examined were 5 mg, 10 mg, and 20 mg. A viability appraisal depended on the Erectile Function (EF) Domain score of the approved International

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