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
125952791 12595279 1 I 20160413 20160721 20160727 20160727 EXP ZA-AMGEN-ZAFSL2016095963 AMGEN 58.00 YR A M Y 0.00000 20160726 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
125952791 12595279 1 PS ARANESP DARBEPOETIN ALFA 1 Subcutaneous 40 MUG, QWK 103951 40 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125952791 12595279 1 Nephrogenic anaemia

Outcome of event

Event ID CASEID OUTC COD
125952791 12595279 DE
125952791 12595279 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125952791 12595279 Haemoglobin abnormal
125952791 12595279 Neoplasm malignant

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
125952791 12595279 1 20101006 0