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

BLOOD GLUCOSE DECREASED ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
RASH ( 3 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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