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

DIARRHOEA ( 10 FDA reports)
ANAEMIA ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
MENINGITIS BACTERIAL ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
CNS VENTRICULITIS ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INFECTION ( 5 FDA reports)
JEJUNAL ULCER ( 5 FDA reports)
SHOCK ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC INJURY ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TRICHOSPORON INFECTION ( 3 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERAL NUTRITION DISORDER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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