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
127558971 12755897 1 I 201401 20160911 20160916 20160916 EXP PHHY2016BR127409 NOVARTIS 55.00 YR F Y 0.00000 20160916 MD BR BR

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
127558971 12755897 1 PS TYKERB LAPATINIB DITOSYLATE 1 Unknown UNK D 22059
127558971 12755897 2 SS TYKERB LAPATINIB DITOSYLATE 1 Unknown UNK D 22059
127558971 12755897 3 SS TRASTUZUMAB TRASTUZUMAB 1 Unknown UNK D 0
127558971 12755897 4 SS CAPECITABINE. CAPECITABINE 1 Unknown UNK D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127558971 12755897 1 Breast cancer metastatic
127558971 12755897 3 Breast cancer metastatic
127558971 12755897 4 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
127558971 12755897 OT
127558971 12755897 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127558971 12755897 Breast cancer metastatic
127558971 12755897 Death
127558971 12755897 Diarrhoea
127558971 12755897 Malignant neoplasm progression
127558971 12755897 Rash

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
127558971 12755897 1 201203 201401 0
127558971 12755897 2 201403 201408 0
127558971 12755897 3 201203 201401 0
127558971 12755897 4 201403 201408 0