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
97870932 9787093 2 F 20100308 20151204 20131228 20160906 EXP GB-ROCHE-1325036 ROCHE 41.00 YR M Y 0.00000 20160906 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
97870932 9787093 1 PS CAPECITABINE. CAPECITABINE 1 Oral 20896
97870932 9787093 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) U 0
97870932 9787093 3 SS SARGRAMOSTIM SARGRAMOSTIM 1 Intradermal U 0
97870932 9787093 4 C MORPHINE SULPHATE MORPHINE SULFATE 1 0
97870932 9787093 5 C CODEINE PHOSPHATE CODEINE PHOSPHATE 1 0
97870932 9787093 6 C LOPERAMIDE LOPERAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97870932 9787093 1 Pancreatic carcinoma metastatic
97870932 9787093 2 Pancreatic carcinoma metastatic
97870932 9787093 3 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
97870932 9787093 DE
97870932 9787093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97870932 9787093 Abdominal distension
97870932 9787093 Ascites
97870932 9787093 Pain
97870932 9787093 Vomiting

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

no results found

Therapies reported

no results found