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

ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
HYPERAMYLASAEMIA ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MALAISE ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
PLEURAL FIBROSIS ( 6 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
RASH ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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