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

RESPIRATORY FAILURE ( 17 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
NEUTROPENIC COLITIS ( 15 FDA reports)
NEUTROPENIA ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
CEREBRAL HAEMORRHAGE ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
PULMONARY HAEMORRHAGE ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
BACTERAEMIA ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
HYPERGLYCAEMIA ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
INFECTION ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CEREBELLAR SYNDROME ( 6 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
LEUKAEMIA RECURRENT ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
CAECITIS ( 5 FDA reports)
COMA ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
FUSARIUM INFECTION ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
PARAPARESIS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SINUSITIS FUNGAL ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
INFECTIVE THROMBOSIS ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PERICARDITIS INFECTIVE ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VTH NERVE INJURY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)

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