Endocrine disruption and the USFDA's Center for Drug Evaluation and Research

Verfasser / Beitragende:
[A. Jacobs, Paul Brown, James Farrelly, J. E. Fisher, D. Morse]
Ort, Verlag, Jahr:
2003
Enthalten in:
Pure and Applied Chemistry, 75/11-12(2003-01-01), 2605-2607
Format:
Artikel (online)
ID: 378861743
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245 0 0 |a Endocrine disruption and the USFDA's Center for Drug Evaluation and Research  |h [Elektronische Daten]  |c [A. Jacobs, Paul Brown, James Farrelly, J. E. Fisher, D. Morse] 
520 3 |a Drugs may have intended or unintended endocrine effects. Drug evaluation may include both in vitro and in vivo evaluations of toxicity and developmental/reproductive effects. After a signal is identified, human relevance is of utmost concern. An integration "tool" that formalizes a weight-of-evidence approach has been developed to assess concern about reproductive/ developmental toxicity to humans. This approach can be used to assess concern about an endocrine disruption signal. A signal alone does not mean a concern for humans. An effect needs to have biologic relevance, and exposure thresholds for effects may exist. Risk/benefit for a particular drug is a clinical decision and may vary by the drug indication. Risk management for an identified concern could include wording in patient communications, tracking distribution or limited distribution, and patient or pregnancy registries. 
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700 1 |a Farrelly  |D James  |u U.S.Food and Drug Administration, HFD-540 5600 Fishers Lane, Rockville, MD 20857,USA  |4 aut 
700 1 |a Fisher  |D J. E.  |u U.S.Food and Drug Administration, HFD-540 5600 Fishers Lane, Rockville, MD 20857,USA  |4 aut 
700 1 |a Morse  |D D.  |u U.S.Food and Drug Administration, HFD-540 5600 Fishers Lane, Rockville, MD 20857,USA  |4 aut 
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