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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125527702 | 12552770 | 2 | F | 20160808 | 20160713 | 20160817 | EXP | US-JNJFOC-20160703702 | JANSSEN | 0.00 | M | Y | 0.00000 | 20160817 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125527702 | 12552770 | 1 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | N | UNKNOWN;UNKNOWN | 0 | 12.5 | UG | MATRIX PATCH | ||||||
| 125527702 | 12552770 | 2 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | N | UNKNOWN;UNKNOWN | 19813 | 25 | UG | MATRIX PATCH | ||||||
| 125527702 | 12552770 | 3 | SS | FENTANYL. | FENTANYL | 1 | Transdermal | U | U | UNKNOWN;UNKNOWN | 19813 | UNSPECIFIED | |||||||
| 125527702 | 12552770 | 4 | SS | FENTANYL. | FENTANYL | 1 | Transdermal | U | 0 | PATCH |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125527702 | 12552770 | 1 | Pain |
| 125527702 | 12552770 | 2 | Pain |
| 125527702 | 12552770 | 3 | Product used for unknown indication |
| 125527702 | 12552770 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125527702 | 12552770 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125527702 | 12552770 | Hospitalisation | |
| 125527702 | 12552770 | Inappropriate schedule of drug administration | |
| 125527702 | 12552770 | Pain | |
| 125527702 | 12552770 | Product adhesion issue | |
| 125527702 | 12552770 | Product quality issue | |
| 125527702 | 12552770 | Surgery | |
| 125527702 | 12552770 | Therapeutic response decreased | |
| 125527702 | 12552770 | Withdrawal syndrome | |
| 125527702 | 12552770 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |