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

ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 120 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 112 FDA reports)
COAGULATION TIME PROLONGED ( 85 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 82 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 82 FDA reports)
DEEP VEIN THROMBOSIS ( 69 FDA reports)
RESPIRATORY FAILURE ( 68 FDA reports)
PULMONARY EMBOLISM ( 63 FDA reports)
HAEMORRHAGE ( 59 FDA reports)
SEPSIS ( 57 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 55 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 54 FDA reports)
THROMBOCYTOPENIA ( 54 FDA reports)
CEREBRAL INFARCTION ( 52 FDA reports)
HYPOTENSION ( 52 FDA reports)
MULTI-ORGAN FAILURE ( 52 FDA reports)
PYREXIA ( 50 FDA reports)
THROMBOSIS ( 50 FDA reports)
ABDOMINAL PAIN ( 44 FDA reports)
ANAEMIA ( 42 FDA reports)
DYSPNOEA ( 41 FDA reports)
COAGULOPATHY ( 39 FDA reports)
PLATELET COUNT DECREASED ( 39 FDA reports)
PNEUMONIA ( 38 FDA reports)
PULMONARY HAEMORRHAGE ( 37 FDA reports)
ATRIAL FIBRILLATION ( 36 FDA reports)
DRUG INTERACTION ( 35 FDA reports)
NAUSEA ( 35 FDA reports)
ANXIETY ( 34 FDA reports)
HYPERTENSION ( 33 FDA reports)
VOMITING ( 33 FDA reports)
RENAL FAILURE ( 30 FDA reports)
PNEUMOTHORAX ( 29 FDA reports)
PROTHROMBIN TIME PROLONGED ( 29 FDA reports)
RENAL FAILURE ACUTE ( 29 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 28 FDA reports)
EOSINOPHIL COUNT INCREASED ( 28 FDA reports)
PULMONARY HYPERTENSION ( 28 FDA reports)
VENA CAVA THROMBOSIS ( 28 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 27 FDA reports)
BRONCHOPNEUMONIA ( 26 FDA reports)
KLEBSIELLA SEPSIS ( 26 FDA reports)
RECTAL HAEMORRHAGE ( 26 FDA reports)
OVERDOSE ( 25 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
DIARRHOEA ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
CARDIO-RESPIRATORY ARREST ( 23 FDA reports)
DUODENAL ULCER ( 23 FDA reports)
RENAL VEIN THROMBOSIS ( 23 FDA reports)
UNRESPONSIVE TO STIMULI ( 23 FDA reports)
CEREBRAL HAEMORRHAGE ( 22 FDA reports)
DRUG INEFFECTIVE ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
HYPOXIA ( 22 FDA reports)
THROMBOSIS IN DEVICE ( 22 FDA reports)
MELAENA ( 21 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
PAIN ( 21 FDA reports)
SKIN DISCOLOURATION ( 21 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 20 FDA reports)
HAEMATEMESIS ( 20 FDA reports)
HEPATIC FAILURE ( 20 FDA reports)
DEATH ( 18 FDA reports)
MOUTH HAEMORRHAGE ( 18 FDA reports)
TONIC CONVULSION ( 18 FDA reports)
DRUG HYPERSENSITIVITY ( 17 FDA reports)
HEADACHE ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 16 FDA reports)
GANGRENE ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
AMNESIA ( 14 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 14 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
COAGULATION TIME ABNORMAL ( 14 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
PROTHROMBIN TIME SHORTENED ( 14 FDA reports)
RENAL FAILURE CHRONIC ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
DELIRIUM ( 13 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
HYPOKALAEMIA ( 13 FDA reports)
LUNG INFILTRATION ( 13 FDA reports)
DIZZINESS ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
EMBOLISM ( 12 FDA reports)
HAEMODYNAMIC INSTABILITY ( 12 FDA reports)
HAEMORRHAGIC INFARCTION ( 12 FDA reports)
INCORRECT DOSE ADMINISTERED ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 11 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CEREBRAL ISCHAEMIA ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
CIRCULATORY COLLAPSE ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
SHOCK ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
FATIGUE ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
INFECTION ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
SHOCK HAEMORRHAGIC ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
BLEEDING TIME PROLONGED ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
RASH ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
ANEURYSM ( 8 FDA reports)
CARDIAC FAILURE ACUTE ( 8 FDA reports)
CARDIOGENIC SHOCK ( 8 FDA reports)
COMPARTMENT SYNDROME ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DEFORMITY ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
EVANS SYNDROME ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
ISCHAEMIA ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 8 FDA reports)
SWELLING ( 8 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 8 FDA reports)
ACTINOMYCES TEST POSITIVE ( 7 FDA reports)
ACUTE PSYCHOSIS ( 7 FDA reports)
BONE DISORDER ( 7 FDA reports)
BREATH ODOUR ( 7 FDA reports)
CANDIDIASIS ( 7 FDA reports)
CERVICAL DYSPLASIA ( 7 FDA reports)
CHRONIC SINUSITIS ( 7 FDA reports)
COLITIS ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
KERATITIS ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
OSTEONECROSIS OF JAW ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PNEUMATOSIS INTESTINALIS ( 7 FDA reports)
PYELOCALIECTASIS ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SPINAL CORD DISORDER ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
VENOUS THROMBOSIS LIMB ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
ANEURYSM RUPTURED ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
ARTERY DISSECTION ( 6 FDA reports)
ASCITES ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BRAIN HERNIATION ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
MYOCARDIAL STRAIN ( 6 FDA reports)
NEUTROPENIC INFECTION ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
UNEVALUABLE EVENT ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
BONE LESION ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CHILLS ( 5 FDA reports)
COMA ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FEAR ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CEREBROVASCULAR DISORDER ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
FAECALITH ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARVOVIRUS INFECTION ( 4 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RADIAL PULSE ABNORMAL ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STRESS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
ABORTION ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GALLBLADDER OEDEMA ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MASS ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
SCAR ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BILE OUTPUT ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIOPULMONARY BYPASS ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
COAGULATION TIME SHORTENED ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALL ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE VASCULITIS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYMPATHOMIMETIC EFFECT ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENTRICULAR DRAINAGE ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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