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

RENAL FAILURE ( 34 FDA reports)
PAIN ( 26 FDA reports)
INJURY ( 25 FDA reports)
UNEVALUABLE EVENT ( 25 FDA reports)
DEATH ( 23 FDA reports)
RENAL FAILURE ACUTE ( 23 FDA reports)
ANXIETY ( 22 FDA reports)
HYPOTENSION ( 22 FDA reports)
ATRIAL FIBRILLATION ( 20 FDA reports)
FEAR ( 18 FDA reports)
THROMBOCYTOPENIA ( 18 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
RENAL INJURY ( 16 FDA reports)
ANHEDONIA ( 15 FDA reports)
EMOTIONAL DISTRESS ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
DEPRESSION ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
DEEP VEIN THROMBOSIS ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
STRESS ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
DIARRHOEA ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
ASTHENIA ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COUGH ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
FACTOR IX INHIBITION ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AMNIOTIC BAND SYNDROME ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOROIDAL DETACHMENT ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RASH ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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