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
126376151 12637615 1 I 20160609 20160809 20160809 PER US-ABBVIE-16P-163-1649361-00 ABBVIE 0.00 F Y 0.00000 20160809 MD 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
126376151 12637615 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Unknown UNKNOWN 18723 TABLET
126376151 12637615 2 SS APTIOM ESLICARBAZEPINE ACETATE 1 Unknown UNKNOWN 0
126376151 12637615 3 SS LYRICA PREGABALIN 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126376151 12637615 1 Seizure
126376151 12637615 2 Seizure
126376151 12637615 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126376151 12637615 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126376151 12637615 Diarrhoea
126376151 12637615 Irritability
126376151 12637615 Malaise
126376151 12637615 Memory impairment
126376151 12637615 Seizure
126376151 12637615 Weight increased

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
126376151 12637615 1 201504 0