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
126967201 12696720 1 I 20091016 20151204 20160830 20160830 EXP GB-ROCHE-1822428 ROCHE 77.00 YR F 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
126967201 12696720 1 PS CAPECITABINE. CAPECITABINE 1 Unknown U 20896
126967201 12696720 2 SS SARGRAMOSTIM SARGRAMOSTIM 1 Unknown U 0
126967201 12696720 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Unknown U 0
126967201 12696720 4 C PARACETAMOL ACETAMINOPHEN 1 0
126967201 12696720 5 C TRAMADOL. TRAMADOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126967201 12696720 1 Pancreatic carcinoma metastatic
126967201 12696720 2 Pancreatic carcinoma metastatic
126967201 12696720 3 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
126967201 12696720 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126967201 12696720 Device occlusion

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

no results found

Therapies reported

no results found