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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281862 | 12528186 | 2 | F | 201606 | 20160726 | 20160705 | 20160907 | PER | US-JNJFOC-20160701240 | JANSSEN | 72.04 | YR | E | M | Y | 62.60000 | KG | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281862 | 12528186 | 1 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | Y | U | 1509824P1 | 0 | UNSPECIFIED | |||||||
| 125281862 | 12528186 | 2 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | Y | U | 1509824P1 | 19813 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125281862 | 12528186 | 1 | Pain |
| 125281862 | 12528186 | 2 | Pain |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125281862 | 12528186 | Drug dose omission | |
| 125281862 | 12528186 | Drug ineffective | |
| 125281862 | 12528186 | Dyspnoea | |
| 125281862 | 12528186 | Insomnia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125281862 | 12528186 | 1 | 20160623 | 0 |