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However, greater sensitivity to medications winsome older individuals should be considered [see Use In Specific Populations] . No adverse effects were observed in a study in which tadalafil was administered orally at doses of 60, 200, and1000 mg/kg/day to juvenile rats on postnatal days 14 to 90. The highest plasma tadalafil exposures (AUC)achieved were approximately 10-fold that observed at the MRHD. In a prenatal/postnatal developmental study in rats, postnatal pup survival decreased following maternal exposure to tadalafil doses greater than 10 times theMRHD based on AUC. Signs of maternal toxicity occurred at doses greater than 16 times the MRHD based onAUC.
Brand-name versions of the drug approved for PAH include Adcirca. Once-daily dosing has not been studied in patients with hepatic impairment