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

OCULAR ICTERUS ( 6 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
PAIN ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
SCLERAL DISORDER ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
FIBROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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