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

ARTHROPATHY ( 5 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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