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DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
TREMOR ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
BONE FISSURE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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