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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126458001 | 12645800 | 1 | I | 201602 | 20160331 | 20160811 | 20160811 | PER | US-ENDO PHARMACEUTICALS INC.-2016-002446 | ENDO | 69.67 | YR | F | Y | 91.71000 | KG | 20160811 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126458001 | 12645800 | 1 | PS | PREDNISONE TABLETS | PREDNISONE | 1 | Oral | U | 40256 | 10 | MG | TABLETS | QD | ||||||
| 126458001 | 12645800 | 2 | SS | PREDNISONE TABLETS | PREDNISONE | 1 | Oral | U | 40256 | TABLETS |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126458001 | 12645800 | 1 | Rheumatoid arthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126458001 | 12645800 | Joint swelling | |
| 126458001 | 12645800 | Pain |
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 |
|---|---|---|---|---|---|---|
| 126458001 | 12645800 | 1 | 201602 | 0 | ||
| 126458001 | 12645800 | 2 | 201602 | 0 |