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DRUG INEFFECTIVE ( 27 FDA reports)
ASPERGILLOSIS ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
CHOLESTASIS ( 6 FDA reports)
DEATH ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
CONVULSION ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORNEAL INFECTION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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