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

INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
BONE MARROW FAILURE ( 8 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
ENDOTOXIC SHOCK ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
REFRACTORY ANAEMIA WITH EXCESS BLASTS IN TRANSFORMATION ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)

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