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
127400981 12740098 1 I 20150331 20160906 20160913 20160913 EXP PHHY2016IN124504 NOVARTIS 56.47 YR F Y 0.00000 20160913 CN COUNTRY NOT SPECIFIED IN

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
127400981 12740098 1 PS TYKERB LAPATINIB DITOSYLATE 1 Oral 1250 MG, QD 5000 MG 22059 1250 MG QD
127400981 12740098 2 SS TYKERB LAPATINIB DITOSYLATE 1 Oral 1000 MG, UNK 5000 MG 22059 1000 MG
127400981 12740098 3 SS CAPECITABINE. CAPECITABINE 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127400981 12740098 1 Breast cancer
127400981 12740098 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127400981 12740098 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127400981 12740098 Asphyxia
127400981 12740098 Back pain
127400981 12740098 Diarrhoea
127400981 12740098 Hot flush
127400981 12740098 Pain in extremity

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
127400981 12740098 1 20150328 0
127400981 12740098 2 201606 0