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

SEPSIS ( 20 FDA reports)
COLITIS ( 20 FDA reports)
PNEUMATOSIS INTESTINALIS ( 20 FDA reports)
PERITONITIS ( 20 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
MOUTH HAEMORRHAGE ( 12 FDA reports)
MEDICATION ERROR ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
MELAENA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)

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