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
126531311 12653131 1 I 20160804 20160815 20160815 EXP US-ALEXION PHARMACEUTICALS INC.-A201605798 ALEXION 0.00 F Y 0.00000 20160815 CN 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
126531311 12653131 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
126531311 12653131 2 C BELATACEPT BELATACEPT 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126531311 12653131 1 Haemolytic uraemic syndrome
126531311 12653131 2 Prophylaxis against transplant rejection

Outcome of event

Event ID CASEID OUTC COD
126531311 12653131 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126531311 12653131 Renal disorder
126531311 12653131 Thrombotic microangiopathy

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found