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
97893862 9789386 2 F 20091023 20151204 20131231 20160831 EXP GB-ROCHE-1326358 ROCHE 60.00 YR M Y 0.00000 20160831 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
97893862 9789386 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAYS 1-21 U 20896 BID
97893862 9789386 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) U 0
97893862 9789386 3 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
97893862 9789386 4 C INSULIN INSULIN NOS 1 0
97893862 9789386 5 C GLICLAZIDE GLICLAZIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97893862 9789386 1 Pancreatic carcinoma
97893862 9789386 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97893862 9789386 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97893862 9789386 Abdominal pain
97893862 9789386 Device related infection
97893862 9789386 Hepatic function abnormal
97893862 9789386 Hyperbilirubinaemia
97893862 9789386 Infection
97893862 9789386 Pancreatitis

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

no results found

Therapies reported

no results found