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

WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
SHOCK ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FALL ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
FLUSHING ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
RASH ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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