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
125310091 12531009 1 I 201601 20160630 20160706 20160706 EXP ZA-AMGEN-ZAFSL2016087080 AMGEN 47.00 YR A F Y 0.00000 20160706 OT ZA ZA

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
125310091 12531009 1 PS ARANESP DARBEPOETIN ALFA 1 Subcutaneous 30 UNK, Q2WK 103951 SOLUTION FOR INJECTION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125310091 12531009 1 Nephrogenic anaemia

Outcome of event

Event ID CASEID OUTC COD
125310091 12531009 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125310091 12531009 Death
125310091 12531009 Haemoglobin abnormal

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
125310091 12531009 1 201508 0