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
111667342 11166734 2 F 20160808 20150605 20160831 PER US-JNJFOC-20150505125 JANSSEN 0.00 A M Y 145.15000 KG 20160831 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
111667342 11166734 1 PS TOPAMAX TOPIRAMATE 1 Oral 200+100MG/ TWICE DAY N 619830 20505 300 MG TABLETS TID
111667342 11166734 2 C TRILEPTAL OXCARBAZEPINE 1 Oral 0 900 MG
111667342 11166734 3 C DEPAKOTE DIVALPROEX SODIUM 1 Unknown 0 UNSPECIFIED
111667342 11166734 4 C NEURONTIN GABAPENTIN 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111667342 11166734 1 Epilepsy
111667342 11166734 2 Sedative therapy
111667342 11166734 3 Epilepsy
111667342 11166734 4 Epilepsy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
111667342 11166734 Appetite disorder
111667342 11166734 Weight decreased

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
111667342 11166734 1 1998 0
111667342 11166734 3 2002 0
111667342 11166734 4 2002 0