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
127498891 12749889 1 I 2014 20160907 20160916 20160916 EXP US-ELI_LILLY_AND_COMPANY-US201609003294 ELI LILLY AND CO 0.00 F Y 0.00000 20160915 CN US US

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
127498891 12749889 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 30 MG, QD Y U 21427 30 MG CAPSULE QD
127498891 12749889 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Y U 21427 CAPSULE
127498891 12749889 3 SS DULOXETINE HYDROCHLORIDE. DULOXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN 0
127498891 12749889 4 SS DULOXETINE HYDROCHLORIDE. DULOXETINE HYDROCHLORIDE 1 0
127498891 12749889 5 C PROTONIX /00661201/ OMEPRAZOLE 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127498891 12749889 1 Depression
127498891 12749889 2 Anxiety
127498891 12749889 3 Depression
127498891 12749889 4 Anxiety

Outcome of event

Event ID CASEID OUTC COD
127498891 12749889 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127498891 12749889 Drug withdrawal syndrome
127498891 12749889 Migraine
127498891 12749889 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
127498891 12749889 1 2008 0