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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126905471 | 12690547 | 1 | I | 20100621 | 20160819 | 20160826 | 20160826 | EXP | US-PURDUE PHARMA-USA-2016-0133068 | PURDUE | 5.00 | YR | M | Y | 0.00000 | 20160826 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126905471 | 12690547 | 1 | PS | OXYCONTIN | OXYCODONE HYDROCHLORIDE | 1 | Oral | UNK | U | U | UNKNOWN | 22272 | PROLONGED-RELEASE TABLET | ||||||
126905471 | 12690547 | 2 | SS | Oxycodone Hydrochloride (similar to NDA 22-272) | OXYCODONE HYDROCHLORIDE | 1 | Oral | UNK | U | U | UNKNOWN | 0 | |||||||
126905471 | 12690547 | 3 | SS | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | UNK | U | U | UNKNOWN | 0 | |||||||
126905471 | 12690547 | 4 | SS | SOMA | CARISOPRODOL | 1 | Unknown | UNK | U | U | UNKNOWN | 0 | |||||||
126905471 | 12690547 | 5 | SS | XANAX | ALPRAZOLAM | 1 | Unknown | UNK | U | U | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126905471 | 12690547 | 1 | Product used for unknown indication |
126905471 | 12690547 | 2 | Product used for unknown indication |
126905471 | 12690547 | 3 | Product used for unknown indication |
126905471 | 12690547 | 4 | Product used for unknown indication |
126905471 | 12690547 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126905471 | 12690547 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126905471 | 12690547 | Hypoxia | |
126905471 | 12690547 | Loss of consciousness | |
126905471 | 12690547 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |