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- W2103397999 abstract "1 The approval was based on data from clinical studies involving more than 2,100 patients that showed that tapentadol provided significant relief of moderate to severe acute pain in adults 18 years of age or older as compared to placebo and is generally well tolerated. 2 The U.S. Drug Enforcement Agency has placed Tapentadol (which is now being marketed as brand name NUCYNTA(TM) (New synthetic)), into Schedule II of the Controlled Substances Act. 3" @default.
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- W2103397999 date "2009-10-01" @default.
- W2103397999 modified "2023-09-23" @default.
- W2103397999 title "Tapentadol - A Novel Analgesic" @default.
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