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

URTICARIA ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
EYE IRRITATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
FALL ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use