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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126295812 | 12629581 | 2 | F | 20151215 | 20160907 | 20160808 | 20160912 | EXP | JP-GLAXOSMITHKLINE-JP2016JPN107785 | GLAXOSMITHKLINE | 4.00 | DEC | M | Y | 0.00000 | 20160912 | CN | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126295812 | 12629581 | 1 | PS | LAMICTAL | LAMOTRIGINE | 1 | Oral | 9375 MG, UNK | Y | 20241 | 9375 | MG | TABLET | ||||||
| 126295812 | 12629581 | 2 | C | UNKNOWN DRUG | UNSPECIFIED INGREDIENT | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126295812 | 12629581 | 1 | Bipolar disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126295812 | 12629581 | HO |
| 126295812 | 12629581 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126295812 | 12629581 | Coma | |
| 126295812 | 12629581 | Intentional overdose | |
| 126295812 | 12629581 | Loss of consciousness | |
| 126295812 | 12629581 | Somnolence | |
| 126295812 | 12629581 | Suicidal ideation | |
| 126295812 | 12629581 | Toxicity to various agents |
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 |
|---|---|---|---|---|---|---|
| 126295812 | 12629581 | 1 | 20151215 | 0 |