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

LIVER DISORDER ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ADHESION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
BACK PAIN ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)

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