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
124637772 12463777 2 F 20150816 20160808 20160614 20160810 EXP PHHY2015FR112958 NOVARTIS 44.55 YR F Y 0.00000 20160810 MD FR FR

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
124637772 12463777 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, DAILY (QD) 850 MG Y 22334 5 MG QD
124637772 12463777 2 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, UNK 850 MG Y 22334 10 MG
124637772 12463777 3 SS AFINITOR EVEROLIMUS 1 Oral 5 MG, DAILY (QD) 850 MG Y 22334 5 MG QD
124637772 12463777 4 SS AROMASIN EXEMESTANE 1 Oral 25 MG, QD 0 25 MG QD
124637772 12463777 5 SS AROMASIN EXEMESTANE 1 Oral UNK, QD 0 QD
124637772 12463777 6 C EXEMESTANE. EXEMESTANE 1 Unknown 25 MG, QD 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124637772 12463777 1 Breast cancer
124637772 12463777 4 Breast cancer metastatic
124637772 12463777 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124637772 12463777 HO
124637772 12463777 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124637772 12463777 Bronchospasm
124637772 12463777 Cardiac failure
124637772 12463777 Dyspnoea
124637772 12463777 Haemoglobin decreased
124637772 12463777 Lung disorder

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
124637772 12463777 1 20150125 0
124637772 12463777 2 20150202 20150629 0
124637772 12463777 3 20150713 0
124637772 12463777 4 20150125 0
124637772 12463777 5 20150202 0