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The EU directive also requires "that all appropriate measures are taken to identify clearly any biological medicinal product prescribed, dispensed, or sold in their territory which is the subject of a suspected adverse reaction report, with due regard to the name of the medicinal product and the batch number" 36.
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There have been no adverse reaction reports involving the latter product, called Hep-Lock heparin flush products.
While adverse reaction reports for dietary supplements are not systematically collected, the Food and Drug Administration's Web site, www.cfsan.fda.gov, has information on recent reports.
A comparison of adverse drug reaction reports from professionals and users, relating to risk of dependence and suicidal behavior with paroxetine.
The F.D.A. panel in 1989 considered only the adverse reaction reports, and not the confirmatory evidence from published clinical trials by independent researchers.
Gathering the relevant reaction reports makes it easy to answer such questions.
Functionalized magnetite nanoparticles were synthesized via a versatile solvothermal reaction reported by Li with a slight modification [21].
After BST's first six months on the market, the FDA had received 96 "adverse reaction" reports from 10,000 farmers.
Finally, an aminocarbonylation reaction reported by Stephen Buchwald allows conversion of aryl halides directly into aryl Weinreb Nahm amides.
The majority of reaction reported were self-limited.
The unique identifier should be included in adverse reaction reporting.
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