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

CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
COLITIS ISCHAEMIC ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
GASTRIC ULCER ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
UROSEPSIS ( 10 FDA reports)
VENTRICULAR FIBRILLATION ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
PAIN ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PERIPHERAL ISCHAEMIA ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
POLYP ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)

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