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

CARDIAC FAILURE ( 4 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use