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
125831003 12583100 3 F 20160711 20160831 20160722 20160921 PER US-ELI_LILLY_AND_COMPANY-US201607006049 ELI LILLY AND CO 25.82 YR M Y 56.69000 KG 20160921 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
125831003 12583100 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 25 MG, UNKNOWN Y 21411 25 MG CAPSULE
125831003 12583100 2 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 40 MG, UNKNOWN Y 21411 40 MG CAPSULE
125831003 12583100 3 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 60 MG, QD Y 21411 60 MG CAPSULE QD
125831003 12583100 4 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Oral 80 MG, EACH MORNING Y 21411 80 MG CAPSULE QD
125831003 12583100 5 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 60 MG, UNKNOWN Y 21411 60 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125831003 12583100 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125831003 12583100 Abdominal pain upper
125831003 12583100 Asthenia
125831003 12583100 Binge eating
125831003 12583100 Fatigue
125831003 12583100 Increased appetite
125831003 12583100 Nausea
125831003 12583100 Pallor
125831003 12583100 Palpitations

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
125831003 12583100 1 201606 0
125831003 12583100 4 20160711 20160721 0