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

UNEVALUABLE EVENT ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
PAIN ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
LOEFFLER'S SYNDROME ( 2 FDA reports)
INJURY ( 2 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
COUGH ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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