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

DIARRHOEA ( 23 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 22 FDA reports)
PYREXIA ( 22 FDA reports)
VOMITING ( 20 FDA reports)
INTERSTITIAL LUNG DISEASE ( 18 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 18 FDA reports)
NAUSEA ( 17 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
BLOOD SODIUM DECREASED ( 12 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 12 FDA reports)
ELECTROLYTE IMBALANCE ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
NEPHROLITHIASIS ( 12 FDA reports)
RENAL TUBULAR DISORDER ( 12 FDA reports)
RESIDUAL URINE ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 10 FDA reports)
MALAISE ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
AXILLARY PAIN ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
SHOCK ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
GASTROINTESTINAL OEDEMA ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
RASH ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 4 FDA reports)
URETERIC DILATATION ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COMA ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC OPERATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATOBILIARY INFECTION ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYLORUS DILATATION ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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