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

CONSTIPATION ( 13 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
ENTEROCOLITIS ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
CHOKING ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
THALAMUS HAEMORRHAGE ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
FALL ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DUODENAL SCARRING ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STUPOR ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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