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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123943153 | 12394315 | 3 | F | 2015 | 20160707 | 20160523 | 20160715 | EXP | CA-PFIZER INC-2015187642 | PFIZER | 58.00 | YR | F | Y | 0.00000 | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123943153 | 12394315 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 12.5 MG, WEEKLY | Y | 11719 | 12.5 | MG | /wk | ||||||
| 123943153 | 12394315 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 20 MG, WEEKLY | Y | 11719 | 20 | MG | /wk | ||||||
| 123943153 | 12394315 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 15 MG, WEEKLY | Y | 11719 | 15 | MG | /wk | ||||||
| 123943153 | 12394315 | 4 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | 1 G, 2X/DAY | Y | 7073 | 1 | G | BID | ||||||
| 123943153 | 12394315 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | UNK | Y | 0 | ||||||||||
| 123943153 | 12394315 | 6 | SS | ORENCIA | ABATACEPT | 1 | UNK | Y | 0 | ||||||||||
| 123943153 | 12394315 | 7 | SS | ARAVA | LEFLUNOMIDE | 1 | 20 MG, DAILY | Y | 0 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123943153 | 12394315 | 1 | Rheumatoid arthritis |
| 123943153 | 12394315 | 4 | Rheumatoid arthritis |
| 123943153 | 12394315 | 5 | Rheumatoid arthritis |
| 123943153 | 12394315 | 6 | Rheumatoid arthritis |
| 123943153 | 12394315 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123943153 | 12394315 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123943153 | 12394315 | Arthropathy | |
| 123943153 | 12394315 | Back disorder | |
| 123943153 | 12394315 | Condition aggravated | |
| 123943153 | 12394315 | Diarrhoea | |
| 123943153 | 12394315 | Drug hypersensitivity | |
| 123943153 | 12394315 | Drug ineffective | |
| 123943153 | 12394315 | Limb asymmetry | |
| 123943153 | 12394315 | Liver function test increased | |
| 123943153 | 12394315 | Rash | |
| 123943153 | 12394315 | Rheumatoid arthritis |
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 |
|---|---|---|---|---|---|---|
| 123943153 | 12394315 | 2 | 200901 | 0 | ||
| 123943153 | 12394315 | 3 | 200901 | 0 | ||
| 123943153 | 12394315 | 4 | 200905 | 201008 | 0 | |
| 123943153 | 12394315 | 6 | 20150510 | 0 | ||
| 123943153 | 12394315 | 7 | 201008 | 0 |