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
126905311 12690531 1 I 201304 20160818 20160826 20160826 EXP FR-ELI_LILLY_AND_COMPANY-FR201608009223 ELI LILLY AND CO 11.00 YR M Y 36.00000 KG 20160825 CN FR FR

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
126905311 12690531 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Oral 18 MG, QD Y U 21411 18 MG CAPSULE QD
126905311 12690531 2 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Oral 18 MG, BID Y U 21411 18 MG CAPSULE BID
126905311 12690531 3 C ORAP PIMOZIDE 1 Unknown 4 MG, UNKNOWN 0 4 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126905311 12690531 1 Tourette's disorder
126905311 12690531 3 Tourette's disorder

Outcome of event

Event ID CASEID OUTC COD
126905311 12690531 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126905311 12690531 Aggression
126905311 12690531 Agitation
126905311 12690531 Anger
126905311 12690531 Insomnia
126905311 12690531 Off label use

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
126905311 12690531 1 201604 0