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
126930391 12693039 1 I 20070818 20151204 20160829 20160829 EXP GB-ROCHE-1821679 ROCHE 75.00 YR F Y 0.00000 20160829 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
126930391 12693039 1 PS CAPECITABINE. CAPECITABINE 1 Unknown U 20896
126930391 12693039 2 SS GEMZAR GEMCITABINE HYDROCHLORIDE 1 Unknown U 0
126930391 12693039 3 C ASPIRIN. ASPIRIN 1 0
126930391 12693039 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
126930391 12693039 5 C PARACETAMOL ACETAMINOPHEN 1 0
126930391 12693039 6 C DEXAMETHASONE. DEXAMETHASONE 1 0
126930391 12693039 7 C DOCUSATE SODIUM. DOCUSATE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126930391 12693039 1 Pancreatic carcinoma
126930391 12693039 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
126930391 12693039 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126930391 12693039 Disease progression

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

no results found

Therapies reported

no results found