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

RENAL FAILURE ACUTE ( 12 FDA reports)
HEPATITIS C ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
PNEUMONIA ( 9 FDA reports)
RENAL FAILURE ( 8 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
SINUS TACHYCARDIA ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
AKINESIA ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
PAIN ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
INJURY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMA URAEMIC ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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