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

CEREBRAL INFARCTION ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
MALLORY-WEISS SYNDROME ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 7 FDA reports)
MYELOID LEUKAEMIA ( 7 FDA reports)
TRANSFUSION REACTION ( 7 FDA reports)
TREMOR ( 7 FDA reports)
HYPOTENSION ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
SPLENOMEGALY ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
EXTREMITY CONTRACTURE ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 5 FDA reports)
PAIN ( 5 FDA reports)
PARAPARESIS ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
SCAR ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEFORMITY ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PURPURA ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN FIBROSIS ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ACIDOSIS ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION ABNORMAL ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINOMA ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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