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
126376981 12637698 1 I 20150825 20160809 20160809 PER US-ABBVIE-15P-163-1452165-00 ABBVIE 0.00 F Y 77.00000 KG 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
126376981 12637698 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Unknown UNKNOWN 18723 TABLET
126376981 12637698 2 SS DILANTIN PHENYTOIN 1 Unknown U 0 100 MG QOD
126376981 12637698 3 SS DILANTIN PHENYTOIN 1 Unknown U 0 200 MG QD
126376981 12637698 4 SS ZARONTIN ETHOSUXIMIDE 1 Unknown U 0
126376981 12637698 5 SS KEPPRA LEVETIRACETAM 1 Unknown U 0
126376981 12637698 6 SS MYSOLINE PRIMIDONE 1 Unknown U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126376981 12637698 1 Product used for unknown indication
126376981 12637698 2 Product used for unknown indication
126376981 12637698 4 Petit mal epilepsy
126376981 12637698 5 Product used for unknown indication
126376981 12637698 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126376981 12637698 Alopecia

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

no results found

Therapies reported

no results found