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

HYPERTENSION ( 11 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
DEATH ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
PAIN ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
FALL ( 4 FDA reports)
MALAISE ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
STRESS ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
COMA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use