The Safety Rates Drug Report

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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
125689791 12568979 1 I 20160713 20160719 20160719 PER PHEH2016US017756 NOVARTIS 0.00 F Y 0.00000 20160719 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
125689791 12568979 1 PS TRILEPTAL OXCARBAZEPINE 1 Unknown 300 MG, BID 21014 300 MG BID
125689791 12568979 2 SS TRILEPTAL OXCARBAZEPINE 1 Unknown 150 MG, BID 21014 150 MG BID
125689791 12568979 3 C TOPAMAX TOPIRAMATE 1 Unknown UNK U 0
125689791 12568979 4 C ELAVIL AMITRIPTYLINE HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125689791 12568979 1 Facial pain
125689791 12568979 3 Product used for unknown indication
125689791 12568979 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125689791 12568979 Fatigue
125689791 12568979 Pain

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
125689791 12568979 1 2013 0
125689791 12568979 3 2001 0
125689791 12568979 4 2001 0