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

ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
PNEUMONIA ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PRURITUS ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
RASH ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
DEATH ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)

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