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
125825871 12582587 1 I 201604 20160719 20160722 20160722 EXP PHHY2016VE100376 NOVARTIS 37.74 YR F Y 0.00000 20160722 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
125825871 12582587 1 PS TEGRETOL CARBAMAZEPINE 1 Oral 0.5 DF, QD 16608 .5 DF TABLET QD
125825871 12582587 2 SS TEGRETOL CARBAMAZEPINE 1 Oral 400 MG, BID (IN THE MORNING AND AT NIGHT) 16608 400 MG TABLET BID
125825871 12582587 3 C NEUROTIN//ACETYLCARNITINE HYDROCHLORIDE 2 Unknown 1200 (UNIT UNSPECIFIED), QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125825871 12582587 1 Neuromyelitis optica spectrum disorder
125825871 12582587 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125825871 12582587 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125825871 12582587 Product use issue
125825871 12582587 Seizure

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
125825871 12582587 1 201604 0