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

CEREBRAL ISCHAEMIA ( 5 FDA reports)
STRIDOR ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
RALES ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
CELL MARKER INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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