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

RENAL IMPAIRMENT ( 25 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 24 FDA reports)
DELIRIUM ( 17 FDA reports)
PYREXIA ( 17 FDA reports)
BRADYCARDIA ( 16 FDA reports)
RASH ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
CONVULSION ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
RENAL FAILURE ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
HYPERGLYCAEMIA ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SHOCK ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
MALAISE ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
VOMITING ( 7 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
SALMONELLA SEPSIS ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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