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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125987731 | 12598773 | 1 | I | 2012 | 20160725 | 20160727 | 20160727 | EXP | CN-GLAXOSMITHKLINE-CN2016GSK107719 | GLAXOSMITHKLINE | 25.00 | YR | F | Y | 0.00000 | 20160727 | CN | CN | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125987731 | 12598773 | 1 | PS | LAMICTAL | LAMOTRIGINE | 1 | Oral | UNK | 20241 | TABLET | |||||||||
| 125987731 | 12598773 | 2 | SS | LAMICTAL | LAMOTRIGINE | 1 | 50 MG, UNK | ZE1196 | 20241 | 50 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125987731 | 12598773 | 1 | Epilepsy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125987731 | 12598773 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125987731 | 12598773 | Amnesia | |
| 125987731 | 12598773 | Anaemia | |
| 125987731 | 12598773 | Disease recurrence | |
| 125987731 | 12598773 | Petit mal epilepsy | |
| 125987731 | 12598773 | Suicidal ideation | |
| 125987731 | 12598773 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 125987731 | 12598773 | 1 | 201206 | 0 |