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

THROMBOCYTOPENIA ( 33 FDA reports)
FEBRILE NEUTROPENIA ( 22 FDA reports)
HYPOTENSION ( 20 FDA reports)
DEHYDRATION ( 15 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
BONE PAIN ( 11 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
ARTHRALGIA ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
EPISTAXIS ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
BACTERAEMIA ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HEPATORENAL SYNDROME ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
COLITIS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLISTER ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use