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

FACTOR VIII INHIBITION ( 609 FDA reports)
DRUG DISPENSING ERROR ( 203 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 203 FDA reports)
HAEMARTHROSIS ( 153 FDA reports)
DRUG INEFFECTIVE ( 145 FDA reports)
HAEMORRHAGE ( 136 FDA reports)
HAEMATOMA ( 90 FDA reports)
MUSCLE HAEMORRHAGE ( 89 FDA reports)
INCREASED TENDENCY TO BRUISE ( 60 FDA reports)
OEDEMA PERIPHERAL ( 56 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 52 FDA reports)
VOMITING ( 43 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 42 FDA reports)
SUBDURAL HAEMATOMA ( 42 FDA reports)
RENAL HAEMATOMA ( 36 FDA reports)
CATHETER RELATED INFECTION ( 34 FDA reports)
MOUTH HAEMORRHAGE ( 34 FDA reports)
ARTHRALGIA ( 32 FDA reports)
DYSPNOEA ( 32 FDA reports)
HAEMOGLOBIN DECREASED ( 32 FDA reports)
JOINT SWELLING ( 32 FDA reports)
DEVICE RELATED INFECTION ( 31 FDA reports)
PYREXIA ( 31 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 30 FDA reports)
INJECTION SITE SWELLING ( 30 FDA reports)
MEDICATION ERROR ( 30 FDA reports)
FALL ( 27 FDA reports)
INJURY ( 27 FDA reports)
ABDOMINAL TENDERNESS ( 26 FDA reports)
CHEST PAIN ( 26 FDA reports)
DRUG EFFECT DECREASED ( 26 FDA reports)
HEADACHE ( 26 FDA reports)
TONGUE HAEMORRHAGE ( 26 FDA reports)
CYANOSIS ( 22 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 21 FDA reports)
DRUG ADMINISTRATION ERROR ( 20 FDA reports)
GASTROENTERITIS NOROVIRUS ( 20 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 20 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 20 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
NAUSEA ( 16 FDA reports)
BLEEDING TIME PROLONGED ( 15 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 15 FDA reports)
COMMINUTED FRACTURE ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
HEAD INJURY ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
MALAISE ( 13 FDA reports)
BACTERAEMIA ( 12 FDA reports)
DEATH ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
HEPATITIS C ( 12 FDA reports)
LACERATION ( 12 FDA reports)
THROAT IRRITATION ( 12 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
FEELING HOT ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BRAIN STEM HAEMORRHAGE ( 8 FDA reports)
ECCHYMOSIS ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HANGOVER ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
MELAENA ( 8 FDA reports)
NECK PAIN ( 8 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 8 FDA reports)
ARTHRITIS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
HYPERLIPIDAEMIA ( 7 FDA reports)
VARICES OESOPHAGEAL ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
FEBRILE CONVULSION ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
LIPOATROPHY ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RHODOCOCCUS INFECTION ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
BILIARY COLIC ( 5 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 4 FDA reports)
APATHY ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 4 FDA reports)
MOYAMOYA DISEASE ( 4 FDA reports)
PAIN ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
AGITATION ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COAGULATION FACTOR INHIBITOR ASSAY ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INHIBITING ANTIBODIES ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MASS ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ACCIDENT ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
FACTOR XIII INHIBITION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLASMIN INHIBITOR INCREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANGER ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG HALF-LIFE REDUCED ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use