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
126707904 12670790 4 F 20160814 20160912 20160822 20160919 EXP PHEH2016US020951 NOVARTIS 92.29 YR F Y 0.00000 20160919 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
126707904 12670790 1 PS TYKERB LAPATINIB DITOSYLATE 1 Oral 6 DF, QD D 22059 6 DF TABLET QD
126707904 12670790 2 SS ARIMIDEX ANASTROZOLE 1 Unknown D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126707904 12670790 1 Breast cancer metastatic
126707904 12670790 2 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
126707904 12670790 DE
126707904 12670790 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126707904 12670790 Asthenia
126707904 12670790 Death
126707904 12670790 Diarrhoea
126707904 12670790 Erythema
126707904 12670790 Fatigue
126707904 12670790 Insomnia
126707904 12670790 Jaundice
126707904 12670790 Joint swelling
126707904 12670790 Metastases to liver
126707904 12670790 Pruritus
126707904 12670790 Rash
126707904 12670790 Rash macular
126707904 12670790 Rash pruritic
126707904 12670790 Yellow skin

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
126707904 12670790 1 20160810 0