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

RETINOIC ACID SYNDROME ( 27 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 21 FDA reports)
SEPSIS ( 17 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
PLASMACYTOMA ( 7 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
DEATH ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDITIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BLEEDING PERIPARTUM ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHLOROMA ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VAGINAL PERFORATION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)

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