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
125397781 12539778 1 I 20160608 20160608 20160708 20160708 EXP JP-ELI_LILLY_AND_COMPANY-JP201606004657 ELI LILLY AND CO 45.00 YR M Y 0.00000 20160708 CN JP JP

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
125397781 12539778 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 20 MG, QD Y 21427 20 MG CAPSULE QD
125397781 12539778 2 SS MORPHINE HYDROCHLORIDE MORPHINE HYDROCHLORIDE 1 Unknown U 0 INJECTION
125397781 12539778 3 SS ROPION FLURBIPROFEN AXETIL 1 Unknown U 0 INJECTION
125397781 12539778 4 C LYRICA PREGABALIN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125397781 12539778 1 Cancer pain
125397781 12539778 2 Cancer pain
125397781 12539778 3 Cancer pain
125397781 12539778 4 Cancer pain

Outcome of event

Event ID CASEID OUTC COD
125397781 12539778 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125397781 12539778 Malignant neoplasm progression
125397781 12539778 Nausea
125397781 12539778 Off label use

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125397781 12539778 1 20160608 20160608 0