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

NAUSEA ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ATELECTASIS ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
MITRAL VALVE CALCIFICATION ( 4 FDA reports)
PAIN ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
PLANTAR FASCIITIS ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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