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
65284412 6528441 2 F 20071214 20121206 20080116 20121231 EXP GB-ROCHE-540873 ROCHE 61.45 YR F Y 0.00000 20121231 MD GB GB

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
65284412 6528441 1 PS Capecitabine 1 ORAL D 20896 Tablet
65284412 6528441 2 SS Oxaliplatin 1 INTRAVENOUS D 0
65284412 6528441 3 SS Cetuximab 1 INTRAVENOUS D 0
65284412 6528441 4 C FELODIPINE 1 ORAL D 0 5 MG
65284412 6528441 5 C METOCLOPRAMID 1 UNKNOWN D 0 10 MG
65284412 6528441 6 C PROPIOMAZINE 1 UNKNOWN D 0 25 MG
65284412 6528441 7 C DALTEPARIN SODIUM 1 SUBCUTANEOUS D 0
65284412 6528441 8 C KODEIN 1 UNKNOWN D 0 530 MG
65284412 6528441 9 C PARACETAMOL 1 UNKNOWN D 0 530 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
65284412 6528441 1 Colorectal cancer
65284412 6528441 2 Colorectal cancer
65284412 6528441 3 Colorectal cancer

Outcome of event

Event ID CASEID OUTC COD
65284412 6528441 HO
65284412 6528441 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
65284412 6528441 Dehydration
65284412 6528441 Diarrhoea
65284412 6528441 Vomiting

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
65284412 6528441 1 20071128 20071212 0
65284412 6528441 2 20071128 20071212 0
65284412 6528441 3 20071128 20071212 0