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

PYREXIA ( 8 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
SEPSIS ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
INFECTION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
RASH ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
COMA ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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