FDA Adverse Event Summary report: N

BREAST IMPLANT, 270 CC

MDR report key: 16541 · Received October 3, 1994

Report

Report Number
MW1003567
Date Received
October 3, 1994
Report Date
September 28, 1994
Manufacturer
DOW CORNING CORP.
Product Code
FTR
Report Source
Voluntary report
Reporter Location
WV, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

RPTR COMPLAINED OF FATIGUE, SLEEPLESSNESS, STIFFNESS, MUSCULOSKELETAL PAIN, RAYNAUD'S, DECREASED STAMINA, DRY EYES AND MOUTH, NUMBNESS AND TINGLING IN FINGERS. INCREASED LYMPH NODES IN ARM PITS AND NECK, PERSONALITY CHANGES, SHE IS IRRITABLE AND MOODY, OCCASIONALLY DEPRESSED, HAD MEMORY PROBLEMS, ATYPICAL CONNECTIVE TISSUE DISEASE/RHEUMATIC SYNDROME/NON-SPECITIC AUTOIMMUNE CONDITION, CAPSULAR CONTRACTURES, HEADACHES, NERVOUSNESS, BREAST TENDERNESS, MUSCLE FATIGUE, SWELLING OF HANDS AND FINGERS, COLD FEET AND HANDS, VISIBLE IMPLANT WRINKLES, WEIGHT GAIN, CAN'T HOLD ARMS OVER HEAD AND CHEST AND SHOULDER PAIN. (ALSO SEE 1003568, 1003569)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BREAST IMPLANT, 270 CC Implant FTR DOW CORNING CORP. HH3782

Patients

Seq Age Sex Outcome Treatment
1 *