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INFUSION RELATED REACTION ( 23 FDA reports)
VOMITING ( 21 FDA reports)
NAUSEA ( 17 FDA reports)
PYREXIA ( 17 FDA reports)
BACK PAIN ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
CHILLS ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
PULMONARY TUBERCULOSIS ( 9 FDA reports)
RASH ( 9 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
CANDIDA PNEUMONIA ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
HEPATITIS ACUTE ( 7 FDA reports)
MALAISE ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
MELAENA ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BODY HEIGHT BELOW NORMAL ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
FALL ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
GASTRIC CANCER RECURRENT ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INFECTIVE ANEURYSM ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
PAIN ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)

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