S Lori Brown

Summary

Affiliation: Food and Drug Administration
Country: USA

Publications

  1. ncbi request reprint Breast implant surveillance reports to the U.S. Food and Drug Administration: maternal-child health problems
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health Food and Drug Administration, Seattle District Office, Bothell, WA 98021 4421, USA
    J Long Term Eff Med Implants 16:281-90. 2006
  2. pmc Silicone gel breast implant adverse event reports to the Food and Drug Administration, 1984-1995
    S L Brown
    Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA
    Public Health Rep 113:535-43. 1998
  3. ncbi request reprint Local anesthetic infusion pump systems adverse events reported to the Food and Drug Administration
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland, USA
    Anesthesiology 100:1305-7. 2004
  4. ncbi request reprint Breast implant adverse events during mammography: reports to the Food and Drug Administration
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland 20850, USA
    J Womens Health (Larchmt) 13:371-8; discussion 379-80. 2004
  5. ncbi request reprint An association of silicone-gel breast implant rupture and fibromyalgia
    S Lori Brown
    US Food and Drug Administration, Epidemiology Branch, Center for Devices and Radiological Health, HFZ 541, 1350 Piccard Drive, Rockville, MD 20850, USA
    Curr Rheumatol Rep 4:293-8. 2002
  6. ncbi request reprint Epidemiology of silicone-gel breast implants
    S Lori Brown
    Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA
    Epidemiology 13:S34-9. 2002
  7. ncbi request reprint Role of serology in the diagnosis of Lyme disease
    S L Brown
    Division of Postmarket Surveillance, Food and Drug Administration, Center for Devices and Radiological Health, Rockville, MD, USA
    JAMA 282:62-6. 1999
  8. ncbi request reprint Adjustable silicone gastric banding adverse events reported to the Food and Drug Administration
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiologic Health, Food and Drug Administration, 1350 Piccard Dr, HFZ 541 Rockville MD 20850, USA
    J Long Term Eff Med Implants 13:509-17. 2003
  9. ncbi request reprint Tumor necrosis factor antagonist therapy and lymphoma development: twenty-six cases reported to the Food and Drug Administration
    S Lori Brown
    Center for Biologics Evaluation and Research, FDA, Rockville, Maryland 20852, USA
    Arthritis Rheum 46:3151-8. 2002
  10. ncbi request reprint Replacement surgery and silicone gel breast implant rupture: self-report by women after mammoplasty
    S Lori Brown
    Epidemiology Branch, Division of Postmarket Surveillance, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland 20850, USA
    J Womens Health Gend Based Med 11:255-64. 2002

Collaborators

Detail Information

Publications16

  1. ncbi request reprint Breast implant surveillance reports to the U.S. Food and Drug Administration: maternal-child health problems
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health Food and Drug Administration, Seattle District Office, Bothell, WA 98021 4421, USA
    J Long Term Eff Med Implants 16:281-90. 2006
    ..An additional 3.5% of reports (n=12) detailed a congenital anomaly believed by the reporter to be caused by breast implants...
  2. pmc Silicone gel breast implant adverse event reports to the Food and Drug Administration, 1984-1995
    S L Brown
    Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA
    Public Health Rep 113:535-43. 1998
    ....
  3. ncbi request reprint Local anesthetic infusion pump systems adverse events reported to the Food and Drug Administration
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland, USA
    Anesthesiology 100:1305-7. 2004
  4. ncbi request reprint Breast implant adverse events during mammography: reports to the Food and Drug Administration
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland 20850, USA
    J Womens Health (Larchmt) 13:371-8; discussion 379-80. 2004
    ..To characterize reports of adverse events occurring during mammography to women with breast implants submitted to the Food and Drug Administration (FDA)...
  5. ncbi request reprint An association of silicone-gel breast implant rupture and fibromyalgia
    S Lori Brown
    US Food and Drug Administration, Epidemiology Branch, Center for Devices and Radiological Health, HFZ 541, 1350 Piccard Drive, Rockville, MD 20850, USA
    Curr Rheumatol Rep 4:293-8. 2002
    ..These findings should also be important for regulatory decision making on silicone-gel breast implants...
  6. ncbi request reprint Epidemiology of silicone-gel breast implants
    S Lori Brown
    Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA
    Epidemiology 13:S34-9. 2002
    ....
  7. ncbi request reprint Role of serology in the diagnosis of Lyme disease
    S L Brown
    Division of Postmarket Surveillance, Food and Drug Administration, Center for Devices and Radiological Health, Rockville, MD, USA
    JAMA 282:62-6. 1999
    ..A negative result on the Western blot or ELISA indicates that there is no serologic evidence of infection by B burgdorferi at the time the sample was drawn...
  8. ncbi request reprint Adjustable silicone gastric banding adverse events reported to the Food and Drug Administration
    S Lori Brown
    Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiologic Health, Food and Drug Administration, 1350 Piccard Dr, HFZ 541 Rockville MD 20850, USA
    J Long Term Eff Med Implants 13:509-17. 2003
    ..The loose connection may cause pain and the device no longer performs as intended when there is a leak...
  9. ncbi request reprint Tumor necrosis factor antagonist therapy and lymphoma development: twenty-six cases reported to the Food and Drug Administration
    S Lori Brown
    Center for Biologics Evaluation and Research, FDA, Rockville, Maryland 20852, USA
    Arthritis Rheum 46:3151-8. 2002
    ..This study was undertaken to investigate the occurrence of lymphoproliferative disorders in patients treated with these agents...
  10. ncbi request reprint Replacement surgery and silicone gel breast implant rupture: self-report by women after mammoplasty
    S Lori Brown
    Epidemiology Branch, Division of Postmarket Surveillance, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland 20850, USA
    J Womens Health Gend Based Med 11:255-64. 2002
    ..The main reason leading up to the surgery and the prevalence of ruptured implants reported after explantation are described...
  11. ncbi request reprint Breast pump adverse events: reports to the food and drug administration
    S Lori Brown
    Division of Postmarket Surveillance, Epidemiology Branch, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, Maryland 20850, USA
    J Hum Lact 21:169-74. 2005
    ..Breast pump adverse events are likely underreported to the FDA. Reporting adverse events is important for improving the design and manufacture of breast pumps and subsequently decreasing adverse events...
  12. ncbi request reprint Surgical stapler-associated fatalities and adverse events reported to the Food and Drug Administration
    S Lori Brown
    Epidemiology Branch, Division of Postmarket Surveillance, Office of Surveillance and Biometrics, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA
    J Am Coll Surg 199:374-81. 2004
    ..The Food and Drug Administration (FDA) regulates surgical staplers as a medical device. Manufacturers and health-care providers report adverse events occurring during the use of surgical staplers to the FDA...
  13. ncbi request reprint Allergic reaction to platinum in silicone breast implants
    Sambasiva R Arepalli
    Division of General, Restorative, and Neurological Devices, Office of Device Evaluation, Food and Drug Administration, Rockville, Maryland 20850, USA
    J Long Term Eff Med Implants 12:299-306. 2002
    ....
  14. ncbi request reprint Life-threatening histoplasmosis complicating immunotherapy with tumor necrosis factor alpha antagonists infliximab and etanercept
    Jong Hoon Lee
    Office of Biostatistics and Epidemiology, Center for Biologics Evaluation and Research, FDA, 1401 Rockville Pike, Rockville, MD 20852 1448, USA
    Arthritis Rheum 46:2565-70. 2002
    ..Because of potential immunosuppression related to use of anti-TNFalpha agents, we sought to identify postlicensure cases of opportunistic infection, including histoplasmosis, in patients treated with these products...
  15. ncbi request reprint MR imaging of extracapsular silicone from breast implants: diagnostic pitfalls
    Wendie A Berg
    Department of Radiology, University of Maryland, University Imaging Center, 419 W Redwood St, Ste 110, Baltimore, MD 21201, USA
    AJR Am J Roentgenol 178:465-72. 2002
    ..We sought to identify pitfalls in recognition of extracapsular silicone on MR imaging...
  16. ncbi request reprint Medical device epidemiology and surveillance: patient safety is the bottom line
    S Lori Brown
    Expert Rev Med Devices 1:1-2. 2004