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

ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
NAUSEA ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
VISION BLURRED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ENDOMETRIAL ADENOMA ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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