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
124332564 12433256 4 F 20160502 20160804 20160603 20160815 EXP BR-ALEXION PHARMACEUTICALS INC-A201603866 ALEXION 35.16 YR F Y 0.00000 20160815 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
124332564 12433256 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, FOR 4 WEEKS P0004601 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
124332564 12433256 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124332564 12433256 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
124332564 12433256 HO
124332564 12433256 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124332564 12433256 Arteriovenous fistula occlusion
124332564 12433256 Arteriovenous fistula thrombosis
124332564 12433256 Chills
124332564 12433256 Fistula inflammation
124332564 12433256 Infection
124332564 12433256 Pain
124332564 12433256 Peripheral swelling
124332564 12433256 Tremor

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
124332564 12433256 1 20150216 20150309 0