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

ANGINA PECTORIS ( 23 FDA reports)
DYSPNOEA ( 23 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
BRADYCARDIA ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 13 FDA reports)
HYPERTENSIVE CRISIS ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
HYPERKALAEMIA ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 10 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
HYPOXIA ( 7 FDA reports)
NON-CARDIAC CHEST PAIN ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ANURIA ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use