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
124979493 12497949 3 F 20160611 20160905 20160626 20160906 EXP PHHY2016CO087217 NOVARTIS 62.78 YR F Y 43.00000 KG 20160906 CN COUNTRY NOT SPECIFIED CO

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
124979493 12497949 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 22334 10 MG TABLET QD
124979493 12497949 2 C FULVESTRANT FULVESTRANT 1 Unknown 0 AMPOULE
124979493 12497949 3 C ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Unknown 0 AMPOULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124979493 12497949 1 Breast cancer metastatic
124979493 12497949 2 Product used for unknown indication
124979493 12497949 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124979493 12497949 OT
124979493 12497949 DE
124979493 12497949 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124979493 12497949 Anaemia
124979493 12497949 Coma
124979493 12497949 Death
124979493 12497949 Fall
124979493 12497949 Hypothyroidism

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
124979493 12497949 1 20160308 0