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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127409571 | 12740957 | 1 | I | 20160901 | 20160914 | 20160914 | EXP | AU-BAUSCH-BL-2016-021245 | BAUSCH AND LOMB | 0.00 | F | Y | 0.00000 | 20160914 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127409571 | 12740957 | 1 | PS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | U | 40070 | ||||||||||
| 127409571 | 12740957 | 2 | SS | METHOTREXATE (METHOTREXATE SODIUM) | METHOTREXATE SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 127409571 | 12740957 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127409571 | 12740957 | 1 | Product used for unknown indication |
| 127409571 | 12740957 | 2 | Product used for unknown indication |
| 127409571 | 12740957 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127409571 | 12740957 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127409571 | 12740957 | Hepatic failure | |
| 127409571 | 12740957 | Intentional product use issue | |
| 127409571 | 12740957 | Pneumocystis jirovecii pneumonia | |
| 127409571 | 12740957 | Sepsis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |