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

DIZZINESS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD INSULIN DECREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
ABASIA ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FALL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)

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