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
97821662 9782166 2 F 20101117 20151204 20131226 20160901 EXP GB-ROCHE-1326010 ROCHE 82.00 YR M Y 0.00000 20160901 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
97821662 9782166 1 PS CAPECITABINE. CAPECITABINE 1 Oral AS PER PROTOCOL U 20896 TABLET BID
97821662 9782166 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) AS PER PROTOCOL U 0
97821662 9782166 3 SS SARGRAMOSTIM SARGRAMOSTIM 1 Intradermal AS PER PROTOCOL U 0
97821662 9782166 4 C OMEPRAZOLE. OMEPRAZOLE 1 0
97821662 9782166 5 C CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 0
97821662 9782166 6 C LATANOPROST. LATANOPROST 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97821662 9782166 1 Pancreatic carcinoma metastatic
97821662 9782166 2 Pancreatic carcinoma metastatic
97821662 9782166 3 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
97821662 9782166 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97821662 9782166 Duodenal stenosis
97821662 9782166 Vomiting
97821662 9782166 Weight decreased

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

no results found

Therapies reported

no results found