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
125203661 12520366 1 I 20160623 20160701 20160701 EXP US-ASTRAZENECA-2016SE70176 ASTRAZENECA 44.00 YR F Y 0.00000 20160701 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
125203661 12520366 1 PS FASLODEX FULVESTRANT 1 Intramuscular U 21344 INJECTION
125203661 12520366 2 SS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous U 0 IMPLANT
125203661 12520366 3 SS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous U 0 IMPLANT
125203661 12520366 4 SS ABRAXANE PACLITAXEL 1 Unknown U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125203661 12520366 1 Breast cancer metastatic
125203661 12520366 4 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
125203661 12520366 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125203661 12520366 Death

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
125203661 12520366 1 201502 0
125203661 12520366 3 201502 0
125203661 12520366 4 201502 0