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
119527145 11952714 5 F 20160107 20160817 20160126 20160826 EXP ES-ALEXION PHARMACEUTICALS INC.-A201600368 ALEXION 27.23 YR M Y 0.00000 20160826 PH ES ES

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
119527145 11952714 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, WEEKLY 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
119527145 11952714 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, BIWEEKLY P0003304 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119527145 11952714 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
119527145 11952714 HO
119527145 11952714 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119527145 11952714 Acute respiratory distress syndrome
119527145 11952714 Anaemia
119527145 11952714 Cardiac failure
119527145 11952714 Diabetic metabolic decompensation
119527145 11952714 Pneumonia cytomegaloviral
119527145 11952714 Renal failure
119527145 11952714 Sepsis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
119527145 11952714 1 20151120 201512 0
119527145 11952714 2 201512 0