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
126930291 12693029 1 I 20071111 20151204 20160829 20160829 EXP GB-ROCHE-1819041 ROCHE 78.00 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
126930291 12693029 1 PS CAPECITABINE. CAPECITABINE 1 Oral U 20896 TABLET
126930291 12693029 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) U 0
126930291 12693029 3 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126930291 12693029 4 C LOSARTAN. LOSARTAN 1 0
126930291 12693029 5 C SIMVASTATIN. SIMVASTATIN 1 0
126930291 12693029 6 C GLICLAZIDE GLICLAZIDE 1 0
126930291 12693029 7 C OMEPRAZOLE. OMEPRAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126930291 12693029 1 Pancreatic carcinoma
126930291 12693029 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
126930291 12693029 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126930291 12693029 Deep vein thrombosis
126930291 12693029 Device occlusion
126930291 12693029 Device related infection
126930291 12693029 Vomiting

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

no results found

Therapies reported

no results found