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
126394931 12639493 1 I 20160727 20160728 20160810 20160810 EXP BR-ALEXION PHARMACEUTICALS INC.-A201605726 ALEXION 13.00 YR M Y 53.00000 KG 20160810 CN BR BR

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
126394931 12639493 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW U 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
126394931 12639493 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126394931 12639493 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W U 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126394931 12639493 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
126394931 12639493 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126394931 12639493 Haemolysis
126394931 12639493 Inappropriate schedule of drug administration
126394931 12639493 Renal impairment
126394931 12639493 Weight increased

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
126394931 12639493 1 20140221 20140428 0
126394931 12639493 2 20140407 0