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210907 r ||| eng |
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|a Clinical review report: Tapentadol hydrochloride extended-release tablet (Nucynta extended-release)
|h Elektronische Ressource
|b (Paladin labs inc.)
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|a Clinical Review Report for Nucynta extended-release
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|a Tapentadol hydrochloride extended-release tablet (Nucynta extended-release)
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|a Final
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|a Ottawa (ON)
|b Canadian Agency for Drugs and Technologies in Health
|c 2018, October 2018
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|a 1 PDF file (161 pages)
|b illustrations
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|a Includes bibliographical references
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a CADTH common drug review
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|a "Indication: Management of pain severe enough to require daily, continuous, long-term opioid treatment, and: that is opioid responsive; and for which alternative treatment options are inadequate. Tapentadol extended-release tablet is not indicated as an as-needed (prn) analgesic."
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|u https://www.ncbi.nlm.nih.gov/books/NBK540241
|3 Volltext
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|a 610
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|a The objective of this review is to perform a systematic review of the beneficial and harmful effects of tapentadol hydrochloride extended-release tablets (Nucynta Extended-Release) 100 mg to 250 mg twice a day for the management of pain severe enough to require daily, continuous, long-term opioid treatment, and: that is opioid responsive; and for which alternative treatment options are inadequate. Nucynta Extended-Release is not indicated as an as-needed analgesic
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