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

WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
RENAL CYST INFECTION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
RECTAL STENOSIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CYSTITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHOKING ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA B VIRUS TEST POSITIVE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)

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