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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124799434 | 12479943 | 4 | F | 2016 | 20160720 | 20160620 | 20160721 | EXP | US-JNJFOC-20160600120 | JANSSEN | 73.70 | YR | E | F | Y | 81.65000 | KG | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124799434 | 12479943 | 1 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | N | UNKNOWN | 19813 | PATCH | ||||||||
| 124799434 | 12479943 | 2 | SS | FENTANYL. | FENTANYL | 1 | Transdermal | Y | N | UNKNOWN | 19813 | MATRIX PATCH | |||||||
| 124799434 | 12479943 | 3 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | N | 1509823P1 | 0 | MATRIX PATCH | ||||||||
| 124799434 | 12479943 | 4 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | N | 1509823P1 | 19813 | MATRIX PATCH | ||||||||
| 124799434 | 12479943 | 5 | C | KEPPRA | LEVETIRACETAM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 124799434 | 12479943 | 6 | C | LYRICA | PREGABALIN | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124799434 | 12479943 | 1 | Pain |
| 124799434 | 12479943 | 2 | Pain |
| 124799434 | 12479943 | 3 | Pain |
| 124799434 | 12479943 | 4 | Pain |
| 124799434 | 12479943 | 5 | Product used for unknown indication |
| 124799434 | 12479943 | 6 | Pain in extremity |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124799434 | 12479943 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124799434 | 12479943 | Application site erosion | |
| 124799434 | 12479943 | Blister | |
| 124799434 | 12479943 | Body height decreased | |
| 124799434 | 12479943 | Diarrhoea | |
| 124799434 | 12479943 | Drug diversion | |
| 124799434 | 12479943 | Pain | |
| 124799434 | 12479943 | Product quality issue | |
| 124799434 | 12479943 | Underdose | |
| 124799434 | 12479943 | Withdrawal syndrome | |
| 124799434 | 12479943 | 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
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 124799434 | 12479943 | 1 | 1991 | 0 | ||
| 124799434 | 12479943 | 2 | 2016 | 2016 | 0 | |
| 124799434 | 12479943 | 3 | 20160603 | 0 | ||
| 124799434 | 12479943 | 4 | 201603 | 0 |