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

NEUTROPENIA ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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