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
116299445 11629944 5 F 201410 20160720 20151014 20160726 EXP BG-ELI_LILLY_AND_COMPANY-BG201510001494 ELI LILLY AND CO 38.00 YR F Y 0.00000 20160726 MD BG BG

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
116299445 11629944 1 PS ZYPREXA OLANZAPINE 1 Oral 10 MG, QD U 20592 10 MG TABLET QD
116299445 11629944 2 SS ZYPREXA OLANZAPINE 1 Oral 5 MG, QD U 20592 5 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116299445 11629944 1 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
116299445 11629944 OT
116299445 11629944 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116299445 11629944 Abdominal pain
116299445 11629944 Antipsychotic drug level increased
116299445 11629944 Intentional product misuse
116299445 11629944 Liver injury
116299445 11629944 Maternal exposure before pregnancy
116299445 11629944 Placental necrosis
116299445 11629944 Suspected counterfeit product

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
116299445 11629944 1 20081001 0
116299445 11629944 2 201410 0