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

CONDITION AGGRAVATED ( 8 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SCAR ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)

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