Please choose an event type to view the corresponding MedsFacts report:

INJECTION SITE INFECTION ( 12 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
INJECTION SITE MASS ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
INJECTION SITE SCAR ( 4 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
INJURY ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INFECTION ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PAIN ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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