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
125995751 12599575 1 I 20160626 20160530 20160727 20160727 EXP PHHY2016CA075373 NOVARTIS 62.35 YR F Y 0.00000 20160727 MD CA CA

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
125995751 12599575 1 PS TYKERB LAPATINIB DITOSYLATE 1 Oral 1250 MG, UNK 22059 1250 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125995751 12599575 1 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
125995751 12599575 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125995751 12599575 Chapped lips
125995751 12599575 Death
125995751 12599575 Diarrhoea

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
125995751 12599575 1 20160509 0