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
125042222 12504222 2 F 201604 20160705 20160628 20160713 EXP CN-ELI_LILLY_AND_COMPANY-CN201606007794 ELI LILLY AND CO 8.00 YR M Y 0.00000 20160713 CN CN CN

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
125042222 12504222 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Oral 0.5 MG/KG, QD U 21411 .5 MG/KG CAPSULE QD
125042222 12504222 2 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Oral 1.2 MG/KG, QD U 21411 1.2 MG/KG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125042222 12504222 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125042222 12504222 OT
125042222 12504222 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125042222 12504222 Drug dose omission
125042222 12504222 Electrocardiogram abnormal
125042222 12504222 Myocarditis
125042222 12504222 Nasopharyngitis
125042222 12504222 Sinus arrhythmia

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
125042222 12504222 1 201603 0
125042222 12504222 2 20160612 0