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

HAEMOGLOBIN DECREASED ( 5 FDA reports)
DIARRHOEA ( 4 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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