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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125503601 | 12550360 | 1 | I | 20160615 | 20160706 | 20160712 | 20160712 | EXP | IT-PFIZER INC-2016335005 | PFIZER | 56.00 | YR | F | Y | 0.00000 | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125503601 | 12550360 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | UNK | U | 21446 | CAPSULE, HARD | ||||||||
| 125503601 | 12550360 | 2 | SS | HALCION | TRIAZOLAM | 1 | Oral | UNK | U | 17892 | TABLET | ||||||||
| 125503601 | 12550360 | 3 | SS | CARBOLITHIUM | LITHIUM CARBONATE | 1 | Oral | UNK | U | 0 | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125503601 | 12550360 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125503601 | 12550360 | Drug abuse | |
| 125503601 | 12550360 | Sopor | |
| 125503601 | 12550360 | Unresponsive to stimuli |
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 |
|---|---|---|---|---|---|---|
| 125503601 | 12550360 | 1 | 20160615 | 20160615 | 0 | |
| 125503601 | 12550360 | 2 | 20160615 | 20160615 | 0 | |
| 125503601 | 12550360 | 3 | 20160615 | 20160615 | 0 |