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
122571542 12257154 2 F 2012 20160831 20160412 20160906 EXP US-ELI_LILLY_AND_COMPANY-US201604000775 ELI LILLY AND CO 0.00 F Y 0.00000 20160906 MD 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
122571542 12257154 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, UNKNOWN U 21427 30 MG CAPSULE
122571542 12257154 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 60 MG, UNKNOWN U 21427 60 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122571542 12257154 1 Depression

Outcome of event

Event ID CASEID OUTC COD
122571542 12257154 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122571542 12257154 Abdominal pain
122571542 12257154 Breath odour
122571542 12257154 Depression
122571542 12257154 Hypersomnia
122571542 12257154 Impaired self-care
122571542 12257154 Laziness
122571542 12257154 Liver disorder
122571542 12257154 Nausea
122571542 12257154 Nervousness
122571542 12257154 Platelet count increased
122571542 12257154 Vomiting

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
122571542 12257154 1 2009 201602 0
122571542 12257154 2 201602 0