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
122877123 12287712 3 F 20160319 20160819 20160420 20160829 EXP NL-ALEXION PHARMACEUTICALS INC-A201602436 ALEXION 47.92 YR F Y 0.00000 20160829 MD NL NL

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
122877123 12287712 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
122877123 12287712 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK, Q2W 125166 CONCENTRATE FOR SOLUTION FOR INFUSION QOW
122877123 12287712 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK, QW 125166 CONCENTRATE FOR SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122877123 12287712 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
122877123 12287712 OT
122877123 12287712 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
122877123 12287712 Haemolysis
122877123 12287712 Infection
122877123 12287712 Interstitial lung disease
122877123 12287712 Neurological decompensation

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
122877123 12287712 1 20160308 0