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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126141181 | 12614118 | 1 | I | 20160414 | 20160721 | 20160802 | 20160802 | EXP | FR-AFSSAPS-PB20160827 | FR-FRI-1000086580 | FOREST | 53.94 | YR | M | Y | 0.00000 | 20160802 | OT | DK | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126141181 | 12614118 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Oral | 21323 | 20 | MG | FILM-COATED TABLET | ||||||||
| 126141181 | 12614118 | 2 | SS | XANAX | ALPRAZOLAM | 1 | Oral | 30 TABLETS TAKEN AT ONCE | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126141181 | 12614118 | 1 | Product used for unknown indication |
| 126141181 | 12614118 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126141181 | 12614118 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126141181 | 12614118 | Coma | |
| 126141181 | 12614118 | 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 |
|---|---|---|---|---|---|---|
| 126141181 | 12614118 | 1 | 20160414 | 20160414 | 0 | |
| 126141181 | 12614118 | 2 | 20160414 | 20160414 | 0 |