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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127847161 | 12784716 | 1 | I | 20160314 | 20160916 | 20160927 | 20160927 | EXP | US-ENDO PHARMACEUTICALS INC.-2016-005765 | ENDO | 70.62 | YR | M | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127847161 | 12784716 | 1 | PS | PREDNISONE TABLETS | PREDNISONE | 1 | Unknown | UP TO 20MG PER DAY | Y | 40256 | UNKNOWN | ||||||||
| 127847161 | 12784716 | 2 | SS | PREDNISONE TABLETS | PREDNISONE | 1 | Unknown | Y | 40256 | 1 | MG | UNKNOWN | BID | ||||||
| 127847161 | 12784716 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | 0 | 5 | MG | UNKNOWN | BID | |||||||
| 127847161 | 12784716 | 4 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | 0 | UNKNOWN | ||||||||||
| 127847161 | 12784716 | 5 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 0 | UNKNOWN | ||||||||||
| 127847161 | 12784716 | 6 | C | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | 0 | UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127847161 | 12784716 | 1 | Product used for unknown indication |
| 127847161 | 12784716 | 3 | Rheumatoid arthritis |
| 127847161 | 12784716 | 4 | Product used for unknown indication |
| 127847161 | 12784716 | 5 | Product used for unknown indication |
| 127847161 | 12784716 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127847161 | 12784716 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127847161 | 12784716 | Blood blister | |
| 127847161 | 12784716 | Increased tendency to bruise | |
| 127847161 | 12784716 | Scratch | |
| 127847161 | 12784716 | Skin atrophy |
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 |
|---|---|---|---|---|---|---|
| 127847161 | 12784716 | 1 | 20141112 | 0 | ||
| 127847161 | 12784716 | 3 | 20160314 | 0 | ||
| 127847161 | 12784716 | 4 | 20141112 | 0 | ||
| 127847161 | 12784716 | 5 | 201511 | 0 |