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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126684361 | 12668436 | 1 | I | 20160503 | 20160819 | 20160819 | EXP | US-PERNIX THERAPEUTICS-2016PT000102 | PERNIX | 0.00 | Y | 0.00000 | 20160818 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126684361 | 12668436 | 1 | PS | HYDROCODONE BITARTRATE. | HYDROCODONE BITARTRATE | 1 | Oral | UNKNOWN | 202880 | TABLET | |||||||||
| 126684361 | 12668436 | 2 | SS | HYDROCODONE BITARTRATE. | HYDROCODONE BITARTRATE | 1 | Nasal | UNK | 202880 | TABLET | |||||||||
| 126684361 | 12668436 | 3 | SS | LYRICA | PREGABALIN | 1 | Unknown | 600 MG, UNKNOWN | UNKNOWN | 0 | 600 | MG | |||||||
| 126684361 | 12668436 | 4 | SS | XANAX | ALPRAZOLAM | 1 | Unknown | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126684361 | 12668436 | 1 | Product used for unknown indication |
| 126684361 | 12668436 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126684361 | 12668436 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126684361 | 12668436 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |