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
126376741 12637674 1 I 20160624 20160809 20160809 PER US-ABBVIE-16P-163-1660980-00 ABBVIE 30.00 YR F Y 0.00000 20160809 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
126376741 12637674 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Unknown U UNKNOWN 18723 TABLET
126376741 12637674 2 SS ZARONTIN ETHOSUXIMIDE 1 Unknown U UNKNOWN 0
126376741 12637674 3 SS LAMICTAL LAMOTRIGINE 1 Unknown U UNKNOWN 0
126376741 12637674 4 SS TOPAMAX TOPIRAMATE 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126376741 12637674 1 Product used for unknown indication
126376741 12637674 2 Seizure
126376741 12637674 3 Product used for unknown indication
126376741 12637674 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126376741 12637674 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126376741 12637674 Amnesia
126376741 12637674 Drug hypersensitivity
126376741 12637674 Rash
126376741 12637674 Stevens-Johnson syndrome
126376741 12637674 Weight increased

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

no results found

Therapies reported

no results found