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
126948931 12694893 1 I 201607 20160823 20160829 20160829 EXP US-MYLANLABS-2016M1035776 MYLAN 0.00 Y 0.00000 20160829 CN 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
126948931 12694893 1 PS LETROZOLE. LETROZOLE 1 UNK 78190
126948931 12694893 2 SS IBRANCE PALBOCICLIB 1 Oral 125 MG, QD Y U 0 125 MG CAPSULE QD
126948931 12694893 3 SS FASLODEX FULVESTRANT 1 UNK Y U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126948931 12694893 1 Breast cancer metastatic
126948931 12694893 2 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
126948931 12694893 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126948931 12694893 Feeling abnormal
126948931 12694893 Hypoaesthesia
126948931 12694893 Peripheral swelling

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
126948931 12694893 1 20160722 0
126948931 12694893 2 2016 0
126948931 12694893 3 20160721 20160721 0