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
93601912 9360191 2 F 20130627 20130621 20130630 EXP HU-ROCHE-1238223 ROCHE 0.00 F Y 0.00000 20130701 OT HU HU

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
93601912 9360191 1 PS Xeloda 1 ORAL D 20896 500 MG BID
93601912 9360191 2 SS Xeloda 1 ORAL D 20896 500 MG BID
93601912 9360191 3 C Cisplatin 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93601912 9360191 1 Gastric cancer
93601912 9360191 3 Gastric cancer

Outcome of event

Event ID CASEID OUTC COD
93601912 9360191 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
93601912 9360191 Asthenia
93601912 9360191 Dizziness
93601912 9360191 Nausea

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
93601912 9360191 1 20130412 201306 0
93601912 9360191 2 201306 0