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

ARTHRALGIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
COMA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
PERIANAL ERYTHEMA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ALOPECIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)

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