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
126308381 12630838 1 I 20160726 20160808 20160808 PER US-ELI_LILLY_AND_COMPANY-US201607011383 ELI LILLY AND CO 0.00 F Y 0.00000 20160808 OT 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
126308381 12630838 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, UNKNOWN U 21427 30 MG CAPSULE
126308381 12630838 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 60 MG, UNKNOWN U 21427 60 MG CAPSULE
126308381 12630838 3 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, UNKNOWN U 21427 30 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126308381 12630838 1 Anxiety
126308381 12630838 2 Panic disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126308381 12630838 Agitation
126308381 12630838 Diarrhoea
126308381 12630838 Dizziness
126308381 12630838 Inappropriate schedule of drug administration
126308381 12630838 Intentional product misuse
126308381 12630838 Intentional self-injury
126308381 12630838 Withdrawal syndrome

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

no results found

Therapies reported

no results found