Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4506835 | 5686240 | I | 4506835-9 | 20041102 | 20041117 | EXP | USA-2004-0017500 | PURDUE PHARMA L.P. | M | N | 20041116 |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4506835 | 1005409447 | PS | OXYCONTIN | 1 | 240 MG Q12H | D | D | 20553 | |||
| 4506835 | 1005444464 | C | NORCO | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4506835 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4506835 | DRUG WITHDRAWAL SYNDROME |
| 4506835 | MYOCARDIAL INFARCTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4506835 | CSM |
Therapies reported
| no results found |