Abstract
Oral phosphodiesterase-5 inhibitors have emerged as the preferred first-line treatment for erectile dysfunction worldwide because of patient convenience, efficacy, and safety. Clinical trials have shown that tadalafil significantly enhances erectile function across a wide range of etiologies and provides a prolonged period of effectiveness independent of food or alcohol. In this review, the pharmacokinetic and pharmacodynamic characteristics, efficacy, and safety of tadalafil are discussed.
MeSH terms
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3',5'-Cyclic-GMP Phosphodiesterases
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Carbolines / therapeutic use*
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Cyclic Nucleotide Phosphodiesterases, Type 5
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Dose-Response Relationship, Drug
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Drug Evaluation
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Erectile Dysfunction / drug therapy*
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Erectile Dysfunction / metabolism
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Humans
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Male
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Phosphodiesterase Inhibitors / therapeutic use*
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Phosphoric Diester Hydrolases / metabolism
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Tadalafil
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Treatment Outcome
Substances
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Carbolines
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Phosphodiesterase Inhibitors
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Tadalafil
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Phosphoric Diester Hydrolases
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3',5'-Cyclic-GMP Phosphodiesterases
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Cyclic Nucleotide Phosphodiesterases, Type 5
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PDE5A protein, human