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
126787321 12678732 1 I 1996 20160811 20160824 20160824 EXP US-ELI_LILLY_AND_COMPANY-US201608006808 ELI LILLY AND CO 0.00 F Y 0.00000 20160823 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
126787321 12678732 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 60 MG, BID 21427 60 MG CAPSULE BID
126787321 12678732 2 C KLONOPIN CLONAZEPAM 1 Unknown UNK, UNKNOWN 0
126787321 12678732 3 C REXULTI BREXPIPRAZOLE 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126787321 12678732 1 Product used for unknown indication
126787321 12678732 2 Anxiety
126787321 12678732 3 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
126787321 12678732 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126787321 12678732 Crying
126787321 12678732 Dizziness
126787321 12678732 Drug dose omission
126787321 12678732 Palpitations
126787321 12678732 Suicidal ideation
126787321 12678732 Weight increased
126787321 12678732 Withdrawal syndrome

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
126787321 12678732 1 1996 201606 0