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

RENAL IMPAIRMENT ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
DYSPHONIA ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
INFECTION ( 6 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
BACK DISORDER ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DRUG ABUSER ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LARYNGOCELE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SURGERY ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
FALL ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCULAR DYSTROPHY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC DYSPLASIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RASH ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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