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
125517091 12551709 1 I 20160515 20160707 20160713 20160713 EXP PHHY2016FR094513 NOVARTIS 25.60 YR F Y 0.00000 20160713 OT 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
125517091 12551709 1 PS TEGRETOL CARBAMAZEPINE 1 Oral 1400 MG, QD U 16608 1400 MG TABLET QD
125517091 12551709 2 I ZEBINIX ESLICARBAZEPINE ACETATE 1 Oral 800 MG, QD 50400 MG Y 0 800 MG QD
125517091 12551709 3 C KEPPRA LEVETIRACETAM 1 Unknown 3000 MG, QD U 0 3000 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125517091 12551709 1 Product used for unknown indication
125517091 12551709 2 Product used for unknown indication
125517091 12551709 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125517091 12551709 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125517091 12551709 Delirium
125517091 12551709 Drug interaction
125517091 12551709 Rash

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
125517091 12551709 2 20160314 20160519 0