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DISSEMINATED INTRAVASCULAR COAGULATION ( 46 FDA reports)
CONDITION AGGRAVATED ( 33 FDA reports)
PNEUMONIA ( 29 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 27 FDA reports)
SEPTIC SHOCK ( 24 FDA reports)
PLATELET COUNT DECREASED ( 23 FDA reports)
MULTI-ORGAN FAILURE ( 21 FDA reports)
RENAL FAILURE ( 20 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
ANAEMIA ( 18 FDA reports)
DISEASE PROGRESSION ( 18 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 17 FDA reports)
HAEMORRHAGE ( 17 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
RESPIRATORY DEPRESSION ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 15 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HAEMORRHAGIC DIATHESIS ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
MALAISE ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
SHOCK ( 9 FDA reports)
ANURIA ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
COMA ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HEPATIC ATROPHY ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
POSTOPERATIVE INFECTION ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ANTITHROMBIN III DECREASED ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BACTERIAL DIARRHOEA ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 5 FDA reports)
MELAENA ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ASPIRATION ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FALL ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HELLP SYNDROME ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ETHANOL GELATION TEST POSITIVE ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PLASMINOGEN DECREASED ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJURY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THREATENED LABOUR ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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