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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126649711 | 12664971 | 1 | I | 2015 | 20160811 | 20160818 | 20160818 | EXP | US-UCBSA-2016031432 | UCB | 0.00 | F | Y | 0.00000 | 20160818 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126649711 | 12664971 | 1 | PS | LEVETIRACETAM. | LEVETIRACETAM | 1 | 500 MG, 2X/DAY (BID) | 21035 | 500 | MG | BID | ||||||||
126649711 | 12664971 | 2 | SS | LEVETIRACETAM. | LEVETIRACETAM | 1 | 750 MG, 2X/DAY (BID) | 21035 | 750 | MG | BID | ||||||||
126649711 | 12664971 | 3 | SS | VIMPAT | LACOSAMIDE | 1 | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126649711 | 12664971 | 1 | Product used for unknown indication |
126649711 | 12664971 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126649711 | 12664971 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126649711 | 12664971 | Abortion spontaneous | |
126649711 | 12664971 | Aura | |
126649711 | 12664971 | Drug ineffective | |
126649711 | 12664971 | Pregnancy |
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 |
---|---|---|---|---|---|---|
126649711 | 12664971 | 1 | 2015 | 0 |