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

DIARRHOEA ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
RENAL FAILURE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
PAIN ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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