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

THROMBOCYTOPENIA ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
NAUSEA ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
RASH ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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