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

HAEMATOMA ( 8 FDA reports)
PYREXIA ( 5 FDA reports)
OFF LABEL USE ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
FALL ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use