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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126146111 | 12614611 | 1 | I | 20160129 | 20160726 | 20160802 | 20160802 | EXP | FR-ABBVIE-16P-056-1690748-00 | ABBVIE | 65.00 | YR | M | Y | 0.00000 | 20160802 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126146111 | 12614611 | 1 | PS | DEPAKINE CHRONO | VALPROATE SODIUM | 1 | Oral | EXTENDED RELEASE | UNKNOWN | 18081 | TABLET | ||||||||
| 126146111 | 12614611 | 2 | SS | KARDEGIC | ASPIRIN LYSINE | 1 | Oral | UNKNOWN | 0 | ORAL POWDER | |||||||||
| 126146111 | 12614611 | 3 | SS | PAROXETINE HYDROCHLORIDE. | PAROXETINE HYDROCHLORIDE | 1 | Oral | UNKNOWN | 0 | ||||||||||
| 126146111 | 12614611 | 4 | SS | ZOPICLONE | ZOPICLONE | 1 | Oral | UNKNOWN | 0 | ||||||||||
| 126146111 | 12614611 | 5 | SS | AMLOR | AMLODIPINE BESYLATE | 1 | Oral | UNKNOWN | 0 | CAPSULE | |||||||||
| 126146111 | 12614611 | 6 | SS | DIAZEPAM. | DIAZEPAM | 1 | Oral | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126146111 | 12614611 | 1 | Suicide attempt |
| 126146111 | 12614611 | 2 | Suicide attempt |
| 126146111 | 12614611 | 3 | Suicide attempt |
| 126146111 | 12614611 | 4 | Suicide attempt |
| 126146111 | 12614611 | 5 | Suicide attempt |
| 126146111 | 12614611 | 6 | Suicide attempt |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126146111 | 12614611 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126146111 | 12614611 | Cough | |
| 126146111 | 12614611 | Drug level increased | |
| 126146111 | 12614611 | Dyspnoea | |
| 126146111 | 12614611 | Sedation |
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 |
|---|---|---|---|---|---|---|
| 126146111 | 12614611 | 1 | 20160128 | 20160128 | 0 | |
| 126146111 | 12614611 | 2 | 20160128 | 20160128 | 0 | |
| 126146111 | 12614611 | 3 | 20160128 | 20160128 | 0 | |
| 126146111 | 12614611 | 4 | 20160128 | 20160128 | 0 | |
| 126146111 | 12614611 | 5 | 20160128 | 20160128 | 0 | |
| 126146111 | 12614611 | 6 | 20160128 | 20160128 | 0 |