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

CARCINOEMBRYONIC ANTIGEN INCREASED ( 6 FDA reports)
FALL ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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