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

DRUG INEFFECTIVE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FACE OEDEMA ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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