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
127162051 12716205 1 I 20160830 20160906 20160906 EXP PHHY2016VE122026 NOVARTIS 0.00 F Y 0.00000 20160906 MD VE VE

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
127162051 12716205 1 PS TRILEPTAL OXCARBAZEPINE 1 Oral 20 CM3, BID (IN THE MORNING AND IN THE AFTERNOON) 21014 BID
127162051 12716205 2 SS TRILEPTAL OXCARBAZEPINE 1 21014
127162051 12716205 3 C VALPRON 2 Unknown U 0
127162051 12716205 4 C EUTIROX LEVOTHYROXINE SODIUM 1 Unknown 250 MG, QD U 0 250 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127162051 12716205 1 Seizure
127162051 12716205 2 Cerebral disorder
127162051 12716205 3 Seizure
127162051 12716205 4 Anxiety

Outcome of event

Event ID CASEID OUTC COD
127162051 12716205 OT
127162051 12716205 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127162051 12716205 Blindness
127162051 12716205 Deafness
127162051 12716205 Product use issue
127162051 12716205 Seizure
127162051 12716205 Speech disorder

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

no results found

Therapies reported

no results found