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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126619081 | 12661908 | 1 | I | 20160508 | 20160811 | 20160817 | 20160817 | EXP | PHHY2016IT111861 | SANDOZ | 44.53 | YR | F | Y | 0.00000 | 20160817 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126619081 | 12661908 | 1 | PS | ALPRAZOLAM. | ALPRAZOLAM | 1 | Oral | UNK, ONCE/SINGLE | 74112 | 1X |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126619081 | 12661908 | 1 | Drug abuse |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126619081 | 12661908 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126619081 | 12661908 | Drug abuse | |
126619081 | 12661908 | Loss of consciousness | |
126619081 | 12661908 | Snoring | |
126619081 | 12661908 | Suicide attempt |
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 |
---|---|---|---|---|---|---|
126619081 | 12661908 | 1 | 20160508 | 20160508 | 0 |