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    Please make sure that Javascript and cookies are enabled on your browser and that you are not blocking them from loading. (Eli Lilly) tadalafil tablets (2.5 mg, 5 mg, 10 mg, 20 mg) for the United States market has been annouced by Teva Pharmaceuticals, in a first-to-file launch. Tadalafil tablets are a phosphodiesterase 5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED), the signs and symptoms of benign prostatic hyperplasia (BPH), and both ED and the signs and symptoms of BPH (ED/BPH). Tadalafil tablets are recommended for use up to 26 weeks when combined with finasteride to initiate BPH treatment. “We’re proud to offer an affordable treatment option for the estimated 30 million men affected by ED, many of whom will also have symptomatic BPH which is estimated to affect 15 million men in the United States,” said Hafrun Fridriksdottir, EVP and Head of Global R&D for Teva, in a prepared statement. The most common adverse reactions reported in clinical trials (≥ 2%) for tadalafil were headache, flushing, dyspepsia, nasal congestion, back pain, myalgia, pain in limb, naspharyngitis, upper respiratory tract infection, cough, diarrhea, urinary tract infection, gastroesophageal reflux disease, abdominal pain, gastroenteritis, and hypertension. Tadalafil tablets are contraindicated in patients using any form of organic nitrate; and in patients with a known serious hypersensitivity to tadalafil. Furthermore, physicians should consider the cardiovascular status of their patients, since there is a degree of cardiac risk associated with sexual activity.

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