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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125829191 | 12582919 | 1 | I | 20160712 | 20160722 | 20160722 | EXP | CA-PFIZER INC-2016353843 | PFIZER | 75.00 | YR | F | Y | 0.00000 | 20160722 | MD | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125829191 | 12582919 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | U | 0 | ||||||||||
| 125829191 | 12582919 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | UNK | U | 11719 | ||||||||||
| 125829191 | 12582919 | 3 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | UNK | U | 7073 | ||||||||||
| 125829191 | 12582919 | 4 | SS | ARAVA | LEFLUNOMIDE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125829191 | 12582919 | 5 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
| 125829191 | 12582919 | 6 | SS | HYDROXYCHLOROQUINE SULFATE. | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 125829191 | 12582919 | 7 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125829191 | 12582919 | 8 | SS | ORENCIA | ABATACEPT | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125829191 | 12582919 | 2 | Rheumatoid arthritis |
| 125829191 | 12582919 | 4 | Rheumatoid arthritis |
| 125829191 | 12582919 | 5 | Rheumatoid arthritis |
| 125829191 | 12582919 | 7 | Rheumatoid arthritis |
| 125829191 | 12582919 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125829191 | 12582919 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125829191 | 12582919 | Drug ineffective | |
| 125829191 | 12582919 | Drug intolerance | |
| 125829191 | 12582919 | Infection | |
| 125829191 | 12582919 | Intraocular pressure increased | |
| 125829191 | 12582919 | Ovarian neoplasm | |
| 125829191 | 12582919 | Pain | |
| 125829191 | 12582919 | Rash | |
| 125829191 | 12582919 | Rheumatoid arthritis | |
| 125829191 | 12582919 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |