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
127129071 12712907 1 I 201404 20160129 20160902 20160902 EXP KR-ELI_LILLY_AND_COMPANY-KR201602000080 ELI LILLY AND CO 0.00 M Y 0.00000 20160902 CN KR KR

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
127129071 12712907 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 10 MG, UNKNOWN N U 21411 10 MG CAPSULE
127129071 12712907 2 I STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 1 DF, UNKNOWN N U 21411 1 DF CAPSULE
127129071 12712907 3 I CONCERTA METHYLPHENIDATE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN N 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127129071 12712907 1 Attention deficit/hyperactivity disorder
127129071 12712907 3 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
127129071 12712907 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127129071 12712907 Abnormal behaviour
127129071 12712907 Anxiety
127129071 12712907 Chronic disease
127129071 12712907 Drug interaction
127129071 12712907 Mental impairment
127129071 12712907 Syncope
127129071 12712907 Tic

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
127129071 12712907 1 201404 201404 0
127129071 12712907 2 2015 2015 0