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
125758392 12575839 2 F 20160714 20160720 20160720 PER US-ELI_LILLY_AND_COMPANY-US201607005400 ELI LILLY AND CO 7.00 YR F Y 0.00000 20160720 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
125758392 12575839 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 10 MG, UNKNOWN Y U 21411 10 MG CAPSULE
125758392 12575839 2 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 25 MG, QD Y U C476711A 21411 25 MG CAPSULE QD
125758392 12575839 3 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 10 MG, BID Y U 21411 10 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125758392 12575839 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125758392 12575839 Anger
125758392 12575839 Drug effect decreased
125758392 12575839 Drug effect increased
125758392 12575839 Fatigue
125758392 12575839 Somnolence

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
125758392 12575839 1 201606 0
125758392 12575839 2 201606 0
125758392 12575839 3 201607 0