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PAIN IN EXTREMITY ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
VOMITING ( 3 FDA reports)
MALAISE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
PAIN ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)

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