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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4368234 | 4009491 | F | 1 | 4368234-2 | 20040517 | 20040525 | EXP | KII-2001-0001693 | PURDUE PHARMA L.P. | F | N | 20040524 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4368234 | 1004907768 | PS | OXYCONTIN | 1 | D | D | 20553 | ||||
| 4368234 | 1004917362 | SS | DURAGESIC | 1 | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4368234 | 1004907768 | PAIN |
| 4368234 | 1004917362 | PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4368234 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4368234 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4368234 | CR |
| 4368234 | HP |
Therapies reported
| no results found |