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
127157051 12715705 1 I 20160830 20160906 20160906 PER US-PFIZER INC-2016411807 PFIZER 58.00 YR F Y 0.00000 20160906 MD US US

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
127157051 12715705 1 PS AROMASIN EXEMESTANE 1 UNK 20753 COATED TABLET
127157051 12715705 2 SS FEMARA LETROZOLE 1 UNK 0
127157051 12715705 3 SS XELODA CAPECITABINE 1 UNK 0
127157051 12715705 4 SS FASLODEX FULVESTRANT 1 UNK 0
127157051 12715705 5 SS AFINITOR EVEROLIMUS 1 UNK 0
127157051 12715705 6 SS ABRAXANE PACLITAXEL 1 UNK 0
127157051 12715705 7 SS DOXIL DOXORUBICIN HYDROCHLORIDE 1 4 CYCLES 0
127157051 12715705 8 SS GEMZAR GEMCITABINE HYDROCHLORIDE 1 UNK, 3 TREATMENTS 0
127157051 12715705 9 SS NAVELBINE VINORELBINE TARTRATE 1 UNK, 3 TREATMENTS 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127157051 12715705 3 Neuropathy peripheral

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127157051 12715705 Disease progression
127157051 12715705 Neoplasm malignant

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
127157051 12715705 1 201311 20140812 0
127157051 12715705 2 20120229 0
127157051 12715705 3 201007 20110517 0
127157051 12715705 4 20120229 20121003 0
127157051 12715705 5 201311 20140812 0
127157051 12715705 6 20141203 20150126 0
127157051 12715705 7 20150312 20150507 0
127157051 12715705 8 201506 20150828 0
127157051 12715705 9 201506 20150828 0