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Appendix E: Glucosamine: Prototype Monograph Summary
Pages 363-366

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From page 363...
... Thus some pertinent information not available to the Committee could be of importance in evaluating safety to determine if use of this dietary supplement ingredient would present an unreasonable risk of illness or injury. Also, the development and review of this prototype was conducted by individuals whose backgrounds are in general aspects of evaluating science and whose expertise is not necessarily focused specifically on this dietary ingredient, although significant additional assistance was provided by consultants with relevant expertise.
From page 364...
... Many of the trials relied only on passive reporting. In the placebo-controlled trials, the incidence of adverse effects among the treatment arms was almost identical, while in the NSAID comparison trials, adverse effect rates were higher among those taking NSAIDs (range of 15­ 35 percent)
From page 365...
... interpretation of animal and human data indicating that very little intact glucosamine is found in the bloodstream following oral ingestion and thus the secretion problems observed following millimolar blood concentrations in rats would not occur in humans following ingestion,2 and (2) lack of many consistent overt serious effects reported in clinical trials.
From page 366...
... . All future trials should have a systematic collection, evaluation, and reporting of adverse events, and key data relevant to addressing the gaps in knowledge should be collected and reported.


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