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

DRUG INTERACTION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
COMA ( 2 FDA reports)
FALL ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
RASH ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ABASIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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