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pubmed-article:10211012pubmed:abstractTextWe studied 90 adults undergoing surgical removal of at least both lower third molar teeth as day cases under standardized general anaesthesia. Patients were allocated randomly (with stratification for surgeon) to receive tenoxicam 40 mg, tenoxicam 20 mg or placebo i.v. at induction of anaesthesia and orally (effervescent tablets) with food on each of the subsequent 2 days. Panadeine (paracetamol 500 mg-codeine 8 mg) was given before operation and was available as needed for pain thereafter, to a limit of two tablets every 4 h. Nefopam i.v. was also available. Efficacy variables and adverse reactions were assessed over 6 days. Over the 6-day period, patients who received tenoxicam reported less pain on rest (area under the curve; P < 0.05) and less disturbance in sleep (P < 0.01) even though they used fewer Panadeine tablets (P < 0.05). Differences between tenoxicam 40 mg and 20 mg were not significant. There was no significant difference in nefopam requirements or side effects, and no adverse event attributable to the study medication.lld:pubmed
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pubmed-article:10211012pubmed:authorpubmed-author:EdwardsJ LJLlld:pubmed
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pubmed-article:10211012pubmed:pagination875-80lld:pubmed
pubmed-article:10211012pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10211012pubmed:articleTitleTenoxicam and paracetamol-codeine combination after oral surgery: a prospective, randomized, double-blind, placebo-controlled study.lld:pubmed
pubmed-article:10211012pubmed:affiliationSt Marks Clinic, Auckland, New Zealand.lld:pubmed
pubmed-article:10211012pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:10211012pubmed:publicationTypeRandomized Controlled Triallld:pubmed
pubmed-article:10211012pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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