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FACTOR VIII INHIBITION ( 31 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 18 FDA reports)
PERITONEAL CYST ( 16 FDA reports)
MEDICAL DEVICE COMPLICATION ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
CONTUSION ( 14 FDA reports)
INFUSION SITE BRUISING ( 14 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
HAEMARTHROSIS ( 9 FDA reports)
HAEMATOMA ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
PAIN ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
VOMITING ( 3 FDA reports)
SWELLING ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
INHIBITING ANTIBODIES ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
ENDOCRINE NEOPLASM ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
IMMUNISATION ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
RASH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
FALL ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR HAEMORRHAGE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)

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