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
124563112 12456311 2 F 20160531 20160816 20160610 20160824 EXP US-ALEXION PHARMACEUTICALS INC-A201604175 ALEXION 62.53 YR M Y 0.00000 20160824 OT 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
124563112 12456311 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, QW U T2-AE7317B01 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
124563112 12456311 2 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
124563112 12456311 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
124563112 12456311 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124563112 12456311 Inappropriate schedule of drug administration
124563112 12456311 Platelet count decreased

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
124563112 12456311 1 20160527 0