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
123692093 12369209 3 F 20160106 20160713 20160513 20160720 EXP PHHO2016GB006815 NOVARTIS 54.00 YR F Y 80.30000 KG 20160720 MD 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
123692093 12369209 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, ALTERNATE DAYS N U 22334 5 MG TABLET
123692093 12369209 2 SS AFINITOR EVEROLIMUS 1 Oral UNK N U 22334 TABLET
123692093 12369209 3 SS ZOMETA ZOLEDRONIC ACID 1 Unknown UNKNOWN N U 0
123692093 12369209 4 SS DENOSUMAB DENOSUMAB 1 Unknown UNKNOWN N U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123692093 12369209 1 Breast cancer
123692093 12369209 3 Metastases to bone
123692093 12369209 4 Metastases to bone

Outcome of event

Event ID CASEID OUTC COD
123692093 12369209 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123692093 12369209 Osteonecrosis of jaw

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
123692093 12369209 1 20130430 20160222 0
123692093 12369209 2 20160317 20160504 0
123692093 12369209 3 20101207 20130430 0
123692093 12369209 4 201305 20151231 0