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
127498861 12749886 1 I 20160811 20160907 20160916 20160916 EXP DE-ELI_LILLY_AND_COMPANY-DE201609003061 ELI LILLY AND CO 0.00 DY Y 0.00000 20160915 CN DE DE

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
127498861 12749886 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Transplacental 30 MG, QD Y U 21427 30 MG CAPSULE QD
127498861 12749886 2 SS AKINETON BIPERIDEN HYDROCHLORIDE 1 Transplacental UNK, UNKNOWN Y 0
127498861 12749886 3 SS RISPERIDONE. RISPERIDONE 1 Transplacental 3 MG, QD U 0 3 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127498861 12749886 1 Bipolar disorder
127498861 12749886 2 Extrapyramidal disorder
127498861 12749886 3 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
127498861 12749886 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127498861 12749886 Foetal exposure during pregnancy
127498861 12749886 Premature baby

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
127498861 12749886 1 201607 0
127498861 12749886 2 201607 0