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
127710761 12771076 1 I 2014 20160914 20160922 20160922 EXP FR-ELI_LILLY_AND_COMPANY-FR201609005530 ELI LILLY AND CO 70.00 YR M Y 0.00000 20160921 MD FR FR

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
127710761 12771076 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, UNKNOWN U 21427 30 MG
127710761 12771076 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 60 MG, UNKNOWN U 21427 60 MG
127710761 12771076 3 C NOCTAMIDE LORMETAZEPAM 1 Unknown UNK UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127710761 12771076 1 Back pain
127710761 12771076 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127710761 12771076 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127710761 12771076 Back disorder
127710761 12771076 Balance disorder
127710761 12771076 Fall
127710761 12771076 Off label use
127710761 12771076 Weight decreased

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
127710761 12771076 1 2014 0
127710761 12771076 2 2015 201606 0