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
97872692 9787269 2 F 20090905 20151204 20131230 20160901 EXP GB-ROCHE-1325734 ROCHE 65.00 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
97872692 9787269 1 PS CAPECITABINE. CAPECITABINE 1 Oral U 20896 BID
97872692 9787269 2 SS SARGRAMOSTIM SARGRAMOSTIM 1 Intradermal DAYS 1, 3 AND 5 IN WEEK 1, ONCE WEEKLY IN WEEKS 2, 3, 4 AND 6, AND THEN ONCE A MONTH U 0
97872692 9787269 3 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) OVER 30 MINUTES ON DAYS ON DAYS 1 8 AND 15 U 0
97872692 9787269 4 C AMITRIPTYLINE AMITRIPTYLINE 1 0
97872692 9787269 5 C OMEPRAZOLE. OMEPRAZOLE 1 0
97872692 9787269 6 C LOPERAMIDE LOPERAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97872692 9787269 1 Pancreatic carcinoma
97872692 9787269 2 Pancreatic carcinoma
97872692 9787269 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97872692 9787269 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97872692 9787269 Device occlusion
97872692 9787269 Fatigue
97872692 9787269 Pyrexia

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

no results found

Therapies reported

no results found