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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125997251 | 12599725 | 1 | I | 20160516 | 20160727 | 20160727 | PER | US-SA-2016SA097351 | AVENTIS | 0.00 | A | F | Y | 0.00000 | 20160727 | LW | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125997251 | 12599725 | 1 | PS | AMBIEN | ZOLPIDEM TARTRATE | 1 | Oral | UNKNOWN | 19908 | 6 | DF | FILM-COATED TABLET | 1X | ||||||
| 125997251 | 12599725 | 2 | SS | XANAX | ALPRAZOLAM | 1 | Unknown | UNKNOWN | 0 | 6 | DF | TABLET | 1X | ||||||
| 125997251 | 12599725 | 3 | SS | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | UNKNOWN | 0 | 6 | DF | TABLET | 1X |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125997251 | 12599725 | 1 | Overdose |
| 125997251 | 12599725 | 2 | Overdose |
| 125997251 | 12599725 | 3 | Overdose |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125997251 | 12599725 | HO |
| 125997251 | 12599725 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125997251 | 12599725 | Drug level increased | |
| 125997251 | 12599725 | Overdose | |
| 125997251 | 12599725 | Toxicity to various agents | |
| 125997251 | 12599725 | Unresponsive to stimuli |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |