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
97849142 9784914 2 F 20080225 20151204 20131227 20160826 EXP GB-ROCHE-1326122 ROCHE 71.00 YR M Y 0.00000 20160826 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
97849142 9784914 1 PS CAPECITABINE. CAPECITABINE 1 Oral AS PER PROTOCOL U 20896 TABLET BID
97849142 9784914 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) AS PER PROTOCOL U 0
97849142 9784914 3 SS SARGRAMOSTIM SARGRAMOSTIM 1 Intradermal AS PER PROTOCOL U 0
97849142 9784914 4 C CODEINE PHOSPHATE CODEINE PHOSPHATE 1 0
97849142 9784914 5 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97849142 9784914 1 Pancreatic carcinoma metastatic
97849142 9784914 2 Pancreatic carcinoma metastatic
97849142 9784914 3 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
97849142 9784914 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97849142 9784914 Device occlusion

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found