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
97849662 9784966 2 F 20080409 20151204 20131227 20160829 EXP GB-ROCHE-1326481 ROCHE 49.00 YR M Y 0.00000 20160829 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
97849662 9784966 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAYS 1-21 U 20896 TABLET BID
97849662 9784966 2 SS SARGRAMOSTIM SARGRAMOSTIM 1 Intradermal U 0
97849662 9784966 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 30 MINUTES ON DAYS 1, 8, AND 15 U 0
97849662 9784966 4 C LANSOPRAZOL LANSOPRAZOLE 1 0
97849662 9784966 5 C CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 0
97849662 9784966 6 C NAPROXEN. NAPROXEN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97849662 9784966 1 Pancreatic carcinoma
97849662 9784966 2 Pancreatic carcinoma
97849662 9784966 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97849662 9784966 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97849662 9784966 Back pain
97849662 9784966 Diarrhoea
97849662 9784966 Dysuria
97849662 9784966 Nausea
97849662 9784966 Oedema peripheral
97849662 9784966 Vomiting

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

no results found

Therapies reported

no results found