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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126446481 | 12644648 | 1 | I | 2013 | 20150713 | 20160811 | 20160811 | PER | US-ENDO PHARMACEUTICALS INC.-2015-001876 | ENDO | 0.00 | M | Y | 82.17000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126446481 | 12644648 | 1 | PS | PREDNISONE TABLETS | PREDNISONE | 1 | Unknown | U | 40256 | 20 | MG | TABLETS | QD | ||||||
| 126446481 | 12644648 | 2 | SS | PREDNISONE TABLETS | PREDNISONE | 1 | U | 40256 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126446481 | 12644648 | 1 | Rheumatoid arthritis |
| 126446481 | 12644648 | 2 | Pulmonary fibrosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126446481 | 12644648 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126446481 | 12644648 | Diabetes mellitus | |
| 126446481 | 12644648 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |