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

DYSPNOEA ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
VOMITING ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ULCER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)

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