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

NEUTROPENIA ( 15 FDA reports)
THROMBOCYTOPENIA ( 14 FDA reports)
OROPHARYNGEAL PAIN ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 13 FDA reports)
HEPATITIS C ( 12 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
CANDIDIASIS ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
SCHIZOPHRENIA ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
NEUTROPHIL COUNT DECREASED ( 6 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
VANISHING BILE DUCT SYNDROME ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
INFECTION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HEPATITIS B DNA INCREASED ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPERM COUNT ZERO ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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