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
97806962 9780696 2 F 20090726 20151204 20131224 20160830 EXP GB-ROCHE-1324296 ROCHE 71.00 YR M Y 0.00000 20160830 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
97806962 9780696 1 PS CAPECITABINE. CAPECITABINE 1 Oral 20896 TABLET BID
97806962 9780696 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0
97806962 9780696 3 C AMLODIPIN AMLODIPINE BESYLATE 1 0
97806962 9780696 4 C PRAVASTATIN. PRAVASTATIN 1 0
97806962 9780696 5 C GLICLAZIDE GLICLAZIDE 1 0
97806962 9780696 6 C TRAMADOL. TRAMADOL 1 0
97806962 9780696 7 C CHLORTHALIDONE. CHLORTHALIDONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97806962 9780696 1 Pancreatic carcinoma
97806962 9780696 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97806962 9780696 DE
97806962 9780696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97806962 9780696 Abdominal pain
97806962 9780696 Myocardial infarction

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

no results found

Therapies reported

no results found