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

HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
DEATH ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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