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

SEPSIS ( 24 FDA reports)
COLITIS ( 24 FDA reports)
CARDIO-RESPIRATORY ARREST ( 24 FDA reports)
MULTI-ORGAN FAILURE ( 21 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
PERITONITIS ( 5 FDA reports)
VOMITING ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
CANDIDIASIS ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
ASCITES ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
ASPIRATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)

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