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

PYREXIA ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RASH ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
B-CELL LYMPHOMA STAGE III ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
LAPAROSCOPIC STERILISATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
T-CELL LYMPHOMA STAGE III ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VENOUS STENT INSERTION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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