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
97872572 9787257 2 F 20110301 20151204 20131230 20160905 EXP GB-ROCHE-1326372 ROCHE 70.00 YR M Y 0.00000 20160905 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
97872572 9787257 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAYS 1 TO 21 U 20896 TABLET BID
97872572 9787257 2 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) OVER 30 MINUTES DAY 1, 8 AND 15 U 0
97872572 9787257 3 C TAMSULOSIN TAMSULOSIN 1 0
97872572 9787257 4 C OMEPRAZOLE. OMEPRAZOLE 1 0
97872572 9787257 5 C MORPHINE SULFATE. MORPHINE SULFATE 1 0
97872572 9787257 6 C BENDROFLUMETHIAZID 2 0
97872572 9787257 7 C DILTIAZEM. DILTIAZEM 1 0
97872572 9787257 8 C RAMIPRIL. RAMIPRIL 1 0
97872572 9787257 9 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
97872572 9787257 10 C ASPIRIN. ASPIRIN 1 0
97872572 9787257 11 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97872572 9787257 1 Pancreatic carcinoma metastatic
97872572 9787257 2 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
97872572 9787257 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97872572 9787257 Obstruction gastric
97872572 9787257 Vomiting

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

no results found

Therapies reported

no results found