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
118318273 11831827 3 F 20160727 20151214 20160802 EXP GB-AMGEN-GBRSL2015130984 AMGEN 0.00 F Y 0.00000 20160801 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
118318273 11831827 1 PS ARANESP DARBEPOETIN ALFA 1 Unknown 40 MUG, UNK 103951 40 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118318273 11831827 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118318273 11831827 HO
118318273 11831827 OT
118318273 11831827 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
118318273 11831827 Adverse event
118318273 11831827 Clostridium difficile infection
118318273 11831827 Death
118318273 11831827 Infection
118318273 11831827 Pneumonia

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

no results found

Therapies reported

no results found