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INFUSION SITE MASS ( 6 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
SOMNOLENCE ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
FALL ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
RASH ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INFUSION SITE ULCER ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE FIBROSIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
NECROTISING PANNICULITIS ( 1 FDA reports)
NODULE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
APATHY ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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