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

PYREXIA ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
MACULAR ISCHAEMIA ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
DEHYDRATION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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