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3. Post-marketing surveillance of adverse reactions to new medicines. Wilson AB Br Med J; 1977 Oct; 2(6093):1001-3. PubMed ID: 922357 [No Abstract] [Full Text] [Related]
4. Monitoring of drugs after marketing. J R Coll Gen Pract; 1983 Jul; 33(252):438-41. PubMed ID: 6887114 [No Abstract] [Full Text] [Related]
5. A prescription for monitoring drugs. Marshall E Science; 1980 Feb; 207(4433):853-5. PubMed ID: 7355265 [No Abstract] [Full Text] [Related]
6. Why do doctors not report adverse drug reactions? Leiper JM; Lawson DH Neth J Med; 1985; 28(12):546-50. PubMed ID: 3911083 [No Abstract] [Full Text] [Related]
7. The case for recording events in clinical trials. Skegg DC; Doll R Br Med J; 1977 Dec; 2(6101):1523-4. PubMed ID: 338116 [TBL] [Abstract][Full Text] [Related]
8. Adverse drug reaction reporting systems: the United Kingdom and the United States. Scott HD; Thacher A; Rosenbaum SE; Waters WJ; Green M R I Med J (1976); 1988 May; 71(5):179-84. PubMed ID: 3387803 [No Abstract] [Full Text] [Related]
9. Are drug companies a little too vigorous? Radcliffe M Nurs Times; 2004 Jul 13-19; 100(28):156. PubMed ID: 15311541 [No Abstract] [Full Text] [Related]
10. A consideration of the guidelines for investigating potential new drugs in humans in the United Kingdom. McGillion FB Methods Find Exp Clin Pharmacol; 1979 Apr; 1(1):45-50. PubMed ID: 552581 [No Abstract] [Full Text] [Related]
12. Compensating the drug victim. Lancet; 1978 Jul; 2(8079):26. PubMed ID: 78220 [No Abstract] [Full Text] [Related]
13. Symposium on drug safety. The role of regulatory agencies and industry in assessment of the safety of drugs for use in man. The situation in the United Kingdom. Cahal DA Can Med Assoc J; 1968 Feb; 98(6):271-5. PubMed ID: 5636096 [No Abstract] [Full Text] [Related]
14. Crying wolf on drug safety. Br Med J (Clin Res Ed); 1982 Jan; 284(6311):219-20. PubMed ID: 6799107 [No Abstract] [Full Text] [Related]