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

MYOCARDIAL INFARCTION ( 215 FDA reports)
THROMBOCYTOPENIA ( 67 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 65 FDA reports)
DRUG INTERACTION ( 49 FDA reports)
CARDIOGENIC SHOCK ( 33 FDA reports)
DEATH ( 28 FDA reports)
THROMBOSIS IN DEVICE ( 27 FDA reports)
HAEMORRHAGE ( 26 FDA reports)
PERICARDIAL EFFUSION ( 23 FDA reports)
DRUG RESISTANCE ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
CARDIAC TAMPONADE ( 20 FDA reports)
SHOCK HAEMORRHAGIC ( 20 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 17 FDA reports)
VENTRICULAR FIBRILLATION ( 17 FDA reports)
VENTRICULAR TACHYCARDIA ( 17 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
MULTI-ORGAN DISORDER ( 16 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 16 FDA reports)
DIARRHOEA ( 15 FDA reports)
CEREBRAL HAEMORRHAGE ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
BRONCHIAL HAEMORRHAGE ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 12 FDA reports)
CORONARY ARTERY THROMBOSIS ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
MYOCARDIAL ISCHAEMIA ( 10 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
ACUTE ABDOMEN ( 8 FDA reports)
AORTIC DISSECTION ( 8 FDA reports)
HAEMATOMA ( 8 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
PERICARDIAL HAEMORRHAGE ( 8 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 8 FDA reports)
TRACHEAL HAEMORRHAGE ( 8 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MYOCARDIAL RUPTURE ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
FALL ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMORRHAGIC ANAEMIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
KOUNIS SYNDROME ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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