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

PAIN ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
CYST ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
COUGH ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
FALL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)

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