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
121921772 12192177 2 F 2016 20160624 20160318 20160703 EXP GB-AMGEN-GBRSL2016031216 AMGEN 66.00 YR E M Y 0.00000 20160703 OT GB GB

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
121921772 12192177 1 PS ARANESP DARBEPOETIN ALFA 1 Unknown 100 MUG, UNK U 103951 100 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121921772 12192177 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121921772 12192177 HO
121921772 12192177 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121921772 12192177 Escherichia infection
121921772 12192177 Haemodialysis
121921772 12192177 Infection
121921772 12192177 Pneumonia

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

no results found

Therapies reported

no results found