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
121974413 12197441 3 F 20160711 20160322 20160726 EXP GB-ALEXION PHARMACEUTICALS INC-A201601873 ALEXION 0.00 F Y 0.00000 20160726 CN GB GB

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
121974413 12197441 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
121974413 12197441 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
121974413 12197441 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121974413 12197441 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
121974413 12197441 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121974413 12197441 Inappropriate schedule of drug administration

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
121974413 12197441 2 20101209 0