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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88497064 | 8849706 | 4 | F | 200112 | 20160824 | 20121019 | 20160901 | EXP | CA-NAPPMUNDI-CAN-2012-0003404 | PURDUE | 25.00 | YR | M | Y | 0.00000 | 20160901 | CN | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88497064 | 8849706 | 1 | PS | OXYCONTIN | OXYCODONE HYDROCHLORIDE | 1 | Unknown | U | 22272 | PROLONGED-RELEASE TABLET | |||||||||
| 88497064 | 8849706 | 2 | SS | OXYCONTIN | OXYCODONE HYDROCHLORIDE | 1 | U | 22272 | PROLONGED-RELEASE TABLET | ||||||||||
| 88497064 | 8849706 | 3 | SS | OXYCONTIN | OXYCODONE HYDROCHLORIDE | 1 | U | 22272 | PROLONGED-RELEASE TABLET | ||||||||||
| 88497064 | 8849706 | 4 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 88497064 | 8849706 | 5 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | U | U | 0 | ||||||||||
| 88497064 | 8849706 | 6 | SS | MORPHINE SULFATE. | MORPHINE SULFATE | 1 | U | U | 0 | ||||||||||
| 88497064 | 8849706 | 7 | SS | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 88497064 | 8849706 | 8 | SS | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | U | U | 0 | ||||||||||
| 88497064 | 8849706 | 9 | SS | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | U | U | 0 | ||||||||||
| 88497064 | 8849706 | 10 | SS | ALCOHOL. | ALCOHOL | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88497064 | 8849706 | 1 | Gastrointestinal pain |
| 88497064 | 8849706 | 2 | Irritable bowel syndrome |
| 88497064 | 8849706 | 3 | Product used for unknown indication |
| 88497064 | 8849706 | 4 | Gastrointestinal pain |
| 88497064 | 8849706 | 5 | Irritable bowel syndrome |
| 88497064 | 8849706 | 6 | Product used for unknown indication |
| 88497064 | 8849706 | 7 | Gastrointestinal pain |
| 88497064 | 8849706 | 8 | Irritable bowel syndrome |
| 88497064 | 8849706 | 9 | Product used for unknown indication |
| 88497064 | 8849706 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88497064 | 8849706 | OT |
| 88497064 | 8849706 | HO |
| 88497064 | 8849706 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88497064 | 8849706 | Accidental overdose | |
| 88497064 | 8849706 | Drug dependence | |
| 88497064 | 8849706 | Drug withdrawal syndrome | |
| 88497064 | 8849706 | Euphoric mood | |
| 88497064 | 8849706 | Hallucination | |
| 88497064 | 8849706 | Substance abuse | |
| 88497064 | 8849706 | Suicide attempt |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |