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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126773251 | 12677325 | 1 | I | 20160806 | 20160816 | 20160823 | 20160823 | EXP | IT-PFIZER INC-2016391511 | PFIZER | 50.00 | YR | F | Y | 0.00000 | 20160823 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126773251 | 12677325 | 1 | PS | XANAX | ALPRAZOLAM | 1 | Oral | 7 MG, DAILY | Y | 18276 | 7 | MG | TABLET | ||||||
| 126773251 | 12677325 | 2 | SS | HALCION | TRIAZOLAM | 1 | Oral | 2 MG, DAILY | Y | 17892 | 2 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126773251 | 12677325 | 1 | Depression |
| 126773251 | 12677325 | 2 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126773251 | 12677325 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126773251 | 12677325 | Impulsive behaviour | |
| 126773251 | 12677325 | Intentional overdose | |
| 126773251 | 12677325 | Intentional self-injury | |
| 126773251 | 12677325 | 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 |
|---|---|---|---|---|---|---|
| 126773251 | 12677325 | 1 | 20130701 | 0 | ||
| 126773251 | 12677325 | 2 | 20130701 | 0 |