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

CROHN'S DISEASE ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 3 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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