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
106509595 10650959 5 F 20121116 20160628 20141215 20160708 EXP JP-ALEXION PHARMACEUTICALS INC.-A201402257 ALEXION 43.00 YR M Y 0.00000 20160708 CN JP JP

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
106509595 10650959 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
106509595 10650959 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W AA8443B01 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
106509595 10650959 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W AB6695B01 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106509595 10650959 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
106509595 10650959 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106509595 10650959 Bile duct stone
106509595 10650959 Bronchitis
106509595 10650959 Headache
106509595 10650959 Prostatitis

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
106509595 10650959 1 20120608 20120629 0
106509595 10650959 2 20120706 0