29 related articles for article (PubMed ID: 9866488)
1. Silicone gel breast implant adverse event reports to the Food and Drug Administration, 1984-1995.
Brown SL; Parmentier CM; Woo EK; Vishnuvajjala RL; Headrick ML
Public Health Rep; 1998; 113(6):535-43. PubMed ID: 9847926
[TBL] [Abstract][Full Text] [Related]
2. Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002: the importance of reporting suspected reactions.
Wysowski DK; Swartz L
Arch Intern Med; 2005 Jun; 165(12):1363-9. PubMed ID: 15983284
[TBL] [Abstract][Full Text] [Related]
3. MedWatch: the FDA medical products reporting program.
Rheinstein PH
Am Fam Physician; 1993 Sep; 48(4):636-8. PubMed ID: 8379493
[No Abstract] [Full Text] [Related]
4. Surgical stapler-associated fatalities and adverse events reported to the Food and Drug Administration.
Brown SL; Woo EK
J Am Coll Surg; 2004 Sep; 199(3):374-81. PubMed ID: 15325606
[TBL] [Abstract][Full Text] [Related]
5. How do pharmaceutical companies handle consumer adverse drug reaction reports? An overview based on a survey of French drug safety managers and officers.
Fleuranceau-Morel P
Pharmacoepidemiol Drug Saf; 2002; 11(1):37-44. PubMed ID: 11998550
[TBL] [Abstract][Full Text] [Related]
6. US Food and Drug Administration: adverse event reporting.
Graham AA
CRNA; 1998 Nov; 9(4):135-8. PubMed ID: 9866488
[TBL] [Abstract][Full Text] [Related]
7. Improving patient care by reporting problems with medical devices.
White GG; Weick-Brady MD; Goldman SA; Gross TP; Kennedy DL; Lucas BS; Merritt K; Naschinski C
CRNA; 1998 Nov; 9(4):139-56. PubMed ID: 9866489
[TBL] [Abstract][Full Text] [Related]
8. The safety of niacin in the US Food and Drug Administration adverse event reporting database.
Alsheikh-Ali AA; Karas RH
Am J Cardiol; 2008 Apr; 101(8A):9B-13B. PubMed ID: 18375244
[TBL] [Abstract][Full Text] [Related]
9. Post-marketing surveillance and adverse drug reactions.
Shani S
Isr Med Assoc J; 1999 Oct; 1(2):117-9. PubMed ID: 10731310
[No Abstract] [Full Text] [Related]
10. Epidural conduction device fractures and complications of retained fragments.
Fischer R
AANA J; 2008 Feb; 76(1):37-40. PubMed ID: 18323318
[TBL] [Abstract][Full Text] [Related]
11. Infusion pump adverse events: experience from medical device reports.
Brown SL; Morrison AE; Parmentier CM; Woo EK; Vishnuvajjala RL
J Intraven Nurs; 1997; 20(1):41-9. PubMed ID: 9060364
[TBL] [Abstract][Full Text] [Related]
12. Postmarketing surveillance and reporting of adverse drug events.
Baer RK
S D J Med; 2004 Jan; 57(1):13-4. PubMed ID: 14964975
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]