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

PYREXIA ( 18 FDA reports)
PNEUMONIA ( 17 FDA reports)
LEUKOPENIA ( 13 FDA reports)
SEPSIS ( 12 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
BLISTER ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
NAUSEA ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
LIP EROSION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
TRANSPLANT FAILURE ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
INFECTION ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY HILUM MASS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CREATININE URINE DECREASED ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLADDER NECROSIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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