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
125166252 12516625 2 F 20160427 20160725 20160630 20160804 EXP GB-TEVA-671112ACC TEVA 0.00 F Y 0.00000 20160805 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
125166252 12516625 1 PS EPIRUBICIN EPIRUBICIN 1 Unknown U 65331
125166252 12516625 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown U 0
125166252 12516625 3 SS FLUOROURACIL. FLUOROURACIL 1 Unknown U 0
125166252 12516625 4 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous U U 0 600 MG SOLUTION FOR INJECTION Q3W
125166252 12516625 5 SS TAXOTERE DOCETAXEL 1 Unknown U 0
125166252 12516625 6 C LETROZOLE. LETROZOLE 1 Oral 2.9 MILLIGRAM DAILY; 0 2.9 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125166252 12516625 1 Breast cancer
125166252 12516625 2 Breast cancer
125166252 12516625 3 Breast cancer
125166252 12516625 4 Breast cancer
125166252 12516625 5 Breast cancer
125166252 12516625 6 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125166252 12516625 OT
125166252 12516625 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125166252 12516625 Colitis
125166252 12516625 Colitis ulcerative
125166252 12516625 Malaise

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
125166252 12516625 4 20150826 20160504 0
125166252 12516625 6 201510 0