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
97806812 9780681 2 F 20090907 20151204 20131224 20160831 EXP GB-ROCHE-1324470 ROCHE 63.00 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
97806812 9780681 1 PS CAPECITABINE. CAPECITABINE 1 Unknown U 20896
97806812 9780681 2 SS SARGRAMOSTIM SARGRAMOSTIM 1 Unknown U 0
97806812 9780681 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Unknown U 0
97806812 9780681 4 C DEXAMETHASONE. DEXAMETHASONE 1 0
97806812 9780681 5 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 0
97806812 9780681 6 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
97806812 9780681 7 C ENOXAPARIN ENOXAPARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97806812 9780681 1 Pancreatic carcinoma metastatic
97806812 9780681 2 Pancreatic carcinoma metastatic
97806812 9780681 3 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
97806812 9780681 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
97806812 9780681 Abdominal pain
97806812 9780681 Intestinal infarction
97806812 9780681 Intestinal perforation

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

no results found

Therapies reported

no results found