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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 75023052 | 7502305 | 2 | F | 2009 | 20090326 | 20100727 | 20160802 | EXP | US-JNJFOC-20091203637 | JANSSEN | 0.00 | A | M | Y | 108.86000 | KG | 20160802 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 75023052 | 7502305 | 1 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | N | 19813 | PATCH | |||||||||
| 75023052 | 7502305 | 2 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | N | 0908033;0919338;0818549 | 0 | MATRIX PATCH | ||||||||
| 75023052 | 7502305 | 3 | SS | DURAGESIC | FENTANYL | 1 | Transdermal | N | 0908033;0919338;0818549 | 19813 | MATRIX PATCH | ||||||||
| 75023052 | 7502305 | 4 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 0 | TABLET | ||||||||||
| 75023052 | 7502305 | 5 | C | PAROXETINE. | PAROXETINE | 1 | Oral | 0 | TABLET | ||||||||||
| 75023052 | 7502305 | 6 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 0 | TABLET | ||||||||||
| 75023052 | 7502305 | 7 | C | LISINOPRIL. | LISINOPRIL | 1 | Oral | 0 | TABLET | ||||||||||
| 75023052 | 7502305 | 8 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Oral | 0 | TABLET | ||||||||||
| 75023052 | 7502305 | 9 | C | CARVEDILOL. | CARVEDILOL | 1 | Oral | 0 | 625 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 75023052 | 7502305 | 1 | Chest pain |
| 75023052 | 7502305 | 2 | Pain |
| 75023052 | 7502305 | 3 | Chest pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 75023052 | 7502305 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 75023052 | 7502305 | Drug effect decreased | |
| 75023052 | 7502305 | Product quality issue | |
| 75023052 | 7502305 | Weight fluctuation |
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 |
|---|---|---|---|---|---|---|
| 75023052 | 7502305 | 1 | 2008 | 2009 | 0 | |
| 75023052 | 7502305 | 2 | 200910 | 0 | ||
| 75023052 | 7502305 | 3 | 200910 | 0 |