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Links from PubMed

Items: 7

1.

The role of litigation in defining drug risks.

Kesselheim AS, Avorn J.

JAMA. 2007 Jan 17;297(3):308-11. No abstract available.

PMID:
17227983
2.

Physicians' liability for adverse drug reactions.

Kaufman MB, Stoukides CA, Campbell NA.

South Med J. 1994 Aug;87(8):780-4. Review.

PMID:
8052883
3.

Adverse drug reactions.

O'Donnell J.

Leg Med. 1994:229-67. Review.

PMID:
7830481
4.

The Food and Drug Administration's Drug Safety Oversight Board: an evolving paradigm for clinical input on drug safety topics.

Grandinetti CA, Osborne SF.

Clin Pharmacol Ther. 2010 Aug;88(2):269-74. doi: 10.1038/clpt.2010.82. Epub 2010 Jun 9. Review. No abstract available.

PMID:
20531466
5.

Processing and evaluation of adverse drug experience reports at the Food and Drug Administration Center for Veterinary Medicine.

Keller WC, Bataller N, Oeller DS.

J Am Vet Med Assoc. 1998 Jul 15;213(2):208-11. Review. No abstract available.

PMID:
9676589
6.

Role of postmarketing surveillance in contemporary medicine.

Woodcock J, Behrman RE, Dal Pan GJ.

Annu Rev Med. 2011;62:1-10. doi: 10.1146/annurev-med-060309-164311. Review.

PMID:
20809798
7.

European Union directives on medicinal products found to be seriously defective.

Griffin JP.

Adverse Drug React Toxicol Rev. 1999 Mar;18(1):3-4. Review. No abstract available.

PMID:
10401519
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