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
127043021 12704302 1 I 20160817 20160831 20160831 PER US-ELI_LILLY_AND_COMPANY-US201608009500 ELI LILLY AND CO 0.00 M Y 0.00000 20160831 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
127043021 12704302 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 100 MG, UNKNOWN N U C494932A 21411 100 MG CAPSULE
127043021 12704302 2 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 80 MG, UNKNOWN N U 21411 80 MG CAPSULE
127043021 12704302 3 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 60 MG, UNKNOWN N U 21411 60 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127043021 12704302 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127043021 12704302 Anxiety
127043021 12704302 Dizziness
127043021 12704302 Dyspnoea
127043021 12704302 Feeling hot
127043021 12704302 Heart rate abnormal
127043021 12704302 Panic attack

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
127043021 12704302 3 20160815 0