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

PNEUMONIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
PYOTHORAX ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRITIS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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