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
126377161 12637716 1 I 20150904 20160809 20160809 PER US-ABBVIE-15P-163-1459665-00 ABBVIE 0.00 M Y 0.00000 20160809 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
126377161 12637716 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Oral U UNKNOWN 18723
126377161 12637716 2 C TRILEPTAL OXCARBAZEPINE 1 Unknown 0
126377161 12637716 3 C VIMPAT LACOSAMIDE 1 Unknown 0
126377161 12637716 4 C ONFI CLOBAZAM 1 Unknown 0
126377161 12637716 5 C TOPAMAX TOPIRAMATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126377161 12637716 1 Seizure
126377161 12637716 2 Product used for unknown indication
126377161 12637716 3 Product used for unknown indication
126377161 12637716 4 Product used for unknown indication
126377161 12637716 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126377161 12637716 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126377161 12637716 Ammonia increased
126377161 12637716 Platelet count decreased
126377161 12637716 Seizure

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found