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

PYREXIA ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLADDER ADENOCARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOBULIN URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT HEPATOBILIARY NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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