The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
112126676 11212667 6 F 20150605 20160812 20150623 20160819 EXP US-ALEXION-A201502124 ALEXION 0.00 F Y 0.00000 20160819 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
112126676 11212667 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U T2-AD5336B01 125166 CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112126676 11212667 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
112126676 11212667 OT
112126676 11212667 HO
112126676 11212667 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112126676 11212667 Abdominal pain
112126676 11212667 Blood creatinine increased
112126676 11212667 Blood lactate dehydrogenase increased
112126676 11212667 Fatigue
112126676 11212667 Fluid overload
112126676 11212667 Haemoglobin decreased
112126676 11212667 Haemolysis
112126676 11212667 Haptoglobin decreased
112126676 11212667 Headache
112126676 11212667 Intestinal obstruction
112126676 11212667 Nasopharyngitis
112126676 11212667 Ovarian cancer recurrent
112126676 11212667 Splenic lesion
112126676 11212667 Tinnitus

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found