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
118343762 11834376 2 F 20160719 20151214 20160722 PER US-ELI_LILLY_AND_COMPANY-US201512002162 ELI LILLY AND CO 0.00 F Y 0.00000 20160722 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
118343762 11834376 1 PS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 80 MG, QD C435369 21411 80 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118343762 11834376 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118343762 11834376 Corneal abrasion
118343762 11834376 Drug dose omission
118343762 11834376 Dry eye
118343762 11834376 Dry mouth
118343762 11834376 Dry skin
118343762 11834376 Eye pain
118343762 11834376 Fatigue
118343762 11834376 Headache
118343762 11834376 Influenza like illness
118343762 11834376 Nausea
118343762 11834376 Pain
118343762 11834376 Visual impairment

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
118343762 11834376 1 20151031 0