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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124249033 | 12424903 | 3 | F | 20160831 | 20160601 | 20160907 | EXP | CA-PFIZER INC-2016281613 | PFIZER | 66.00 | YR | F | Y | 0.00000 | 20160907 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124249033 | 12424903 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, WEEKLY | 0 | 50 | MG | /wk | |||||||
| 124249033 | 12424903 | 2 | PS | SULFASALAZINE. | SULFASALAZINE | 1 | 1 G, 2X/DAY | 7073 | 1 | G | BID | ||||||||
| 124249033 | 12424903 | 3 | SS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | 1 G, UNK | 0 | 1 | G | ||||||||
| 124249033 | 12424903 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 200 MG, 2X/DAY | 0 | 200 | MG | BID | ||||||||
| 124249033 | 12424903 | 5 | SS | ARAVA | LEFLUNOMIDE | 1 | 20 MG, DAILY | 0 | 20 | MG | |||||||||
| 124249033 | 12424903 | 6 | C | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, DAILY | 0 | 200 | MG | ||||||||
| 124249033 | 12424903 | 7 | C | PREDNISONE. | PREDNISONE | 1 | 8 MG, DAILY | 0 | 8 | MG | |||||||||
| 124249033 | 12424903 | 8 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 25 MG, WEEKLY | 0 | 25 | MG | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124249033 | 12424903 | 1 | Rheumatoid arthritis |
| 124249033 | 12424903 | 2 | Rheumatoid arthritis |
| 124249033 | 12424903 | 6 | Rheumatoid arthritis |
| 124249033 | 12424903 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124249033 | 12424903 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124249033 | 12424903 | Abasia | |
| 124249033 | 12424903 | Cough | |
| 124249033 | 12424903 | Drug ineffective | |
| 124249033 | 12424903 | Hypoaesthesia | |
| 124249033 | 12424903 | Pharyngeal oedema | |
| 124249033 | 12424903 | Rash |
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 |
|---|---|---|---|---|---|---|
| 124249033 | 12424903 | 1 | 2007 | 2007 | 0 | |
| 124249033 | 12424903 | 3 | 2005 | 0 | ||
| 124249033 | 12424903 | 8 | 2004 | 0 |