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

PYREXIA ( 29 FDA reports)
PNEUMOTHORAX ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 16 FDA reports)
DIARRHOEA ( 16 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
VOMITING ( 13 FDA reports)
LIVER DISORDER ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
BRONCHITIS ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
CONVULSION ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
RASH ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
SPUTUM INCREASED ( 8 FDA reports)
SPUTUM PURULENT ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 7 FDA reports)
ASCITES ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
DEVICE RELATED INFECTION ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
MELAENA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 6 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARNITINE DECREASED ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
COUGH ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANTITHROMBIN III DECREASED ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALVEOLAR PROTEINOSIS ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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