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
123220263 12322026 3 F 20160408 20160711 20160502 20160715 EXP JP-GLAXOSMITHKLINE-JP2016JPN058840 GLAXOSMITHKLINE 20.14 YR F Y 0.00000 20160715 CN JP JP

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
123220263 12322026 1 PS LAMICTAL LAMOTRIGINE 1 Oral 25 MG, QOD 225 MG Y 20241 25 MG TABLET QOD
123220263 12322026 2 SS LAMICTAL LAMOTRIGINE 1 Oral 25 MG, 1D 225 MG Y 20241 25 MG TABLET QD
123220263 12322026 3 SS LAMICTAL LAMOTRIGINE 1 Oral 50 MG, 1D 225 MG Y 20241 50 MG TABLET QD
123220263 12322026 4 C SELENICA-R VALPROATE SODIUM 1 200 MG, TID 0 200 MG TID
123220263 12322026 5 C SELENICA-R VALPROATE SODIUM 1 200 UNK, QD 0 200 MG QD
123220263 12322026 6 C SELENICA-R VALPROATE SODIUM 1 600 MG, 1D 0 600 MG QD
123220263 12322026 7 C E KEPPRA LEVETIRACETAM 1 0
123220263 12322026 8 C DEPAKENE VALPROIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123220263 12322026 1 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
123220263 12322026 HO
123220263 12322026 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123220263 12322026 Drug eruption
123220263 12322026 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
123220263 12322026 1 20160315 20160329 0
123220263 12322026 2 20160330 20160408 0
123220263 12322026 3 20160408 20160408 0
123220263 12322026 5 20160315 0
123220263 12322026 6 20160325 0