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
123133866 12313386 6 F 20160330 20160815 20160428 20160822 EXP PHHY2016DE055661 NOVARTIS 0.00 A F Y 82.00000 KG 20160822 MD DE DE

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
123133866 12313386 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 75 MG N 22334 5 MG TABLET QD
123133866 12313386 2 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 75 MG N 22334 10 MG TABLET QD
123133866 12313386 3 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 154.4 MG, QW 1235 MG U 0 154.4 MG /wk
123133866 12313386 4 C EXEMESTANE. EXEMESTANE 1 Oral 25 MG, QD 375 MG N 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123133866 12313386 1 Breast cancer metastatic
123133866 12313386 3 Product used for unknown indication
123133866 12313386 4 Breast cancer metastatic

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123133866 12313386 Fatigue
123133866 12313386 Headache
123133866 12313386 Myalgia

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
123133866 12313386 1 20160316 20160331 0
123133866 12313386 2 20160401 20160512 0
123133866 12313386 3 20110413 20110608 0
123133866 12313386 4 20160316 20160512 0