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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126363261 | 12636326 | 1 | I | 200803 | 20160621 | 20160809 | 20160809 | PER | US-ABBVIE-16P-163-1658555-00 | ABBVIE | 23.72 | YR | M | Y | 0.00000 | 20160809 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126363261 | 12636326 | 1 | PS | DEPAKOTE ER | DIVALPROEX SODIUM | 1 | Oral | AT NIGHT | U | UNKNOWN | 21168 | 2000 | MG | TABLET | QD | ||||
126363261 | 12636326 | 2 | SS | DEPAKOTE ER | DIVALPROEX SODIUM | 1 | Oral | AT NIGHT | U | UNKNOWN | 21168 | 1 | G | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126363261 | 12636326 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126363261 | 12636326 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126363261 | 12636326 | Disturbance in attention | |
126363261 | 12636326 | Fatigue | |
126363261 | 12636326 | Poor quality sleep | |
126363261 | 12636326 | Road traffic accident | |
126363261 | 12636326 | Seizure | |
126363261 | 12636326 | Stress |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |