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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125287901 | 12528790 | 1 | I | 20150525 | 20160705 | 20160705 | EXP | CA-PFIZER INC-2015179918 | PFIZER | 74.00 | YR | F | Y | 0.00000 | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125287901 | 12528790 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 15 MG ( 6 TABLETS OF 2.5 MG), WEEKLY | N | 11719 | 15 | MG | TABLET | /wk | |||||
| 125287901 | 12528790 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 17.5 MG (7 TABLETS OF 2.5 MG) , WEEKLY | N | 11719 | 17.5 | MG | TABLET | /wk | |||||
| 125287901 | 12528790 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 20 MG (8 TABLETS OF 2.5 MG), WEEKLY | N | 11719 | 20 | MG | TABLET | /wk | |||||
| 125287901 | 12528790 | 4 | SS | ARAVA | LEFLUNOMIDE | 1 | 20 MG, DAILY | N | 0 | 20 | MG | TABLET | |||||||
| 125287901 | 12528790 | 5 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 200 MG TABLET TAKE 2 TABLETS DAILY FROM MONDAY TO FRIDAY THEN 1 TABLET DAILY SATURDAY AND SUNDAY | N | 0 | 200 | MG | TABLET | |||||||
| 125287901 | 12528790 | 6 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 400 MG (200 MG X 2 TABLETS), 1X/DAY | N | 0 | 400 | MG | TABLET | QD | ||||||
| 125287901 | 12528790 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 5 MG, DAILY (6 DAYS PER WEEK) | 0 | 5 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125287901 | 12528790 | 1 | Rheumatoid arthritis |
| 125287901 | 12528790 | 4 | Rheumatoid arthritis |
| 125287901 | 12528790 | 5 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125287901 | 12528790 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125287901 | 12528790 | Breast cancer female | |
| 125287901 | 12528790 | Diarrhoea | |
| 125287901 | 12528790 | Drug ineffective | |
| 125287901 | 12528790 | Interstitial lung disease | |
| 125287901 | 12528790 | Mycobacterium tuberculosis complex test positive | |
| 125287901 | 12528790 | Pain | |
| 125287901 | 12528790 | Synovitis |
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 |
|---|---|---|---|---|---|---|
| 125287901 | 12528790 | 1 | 20140818 | 2014 | 0 | |
| 125287901 | 12528790 | 2 | 2014 | 2014 | 0 | |
| 125287901 | 12528790 | 3 | 20141125 | 201602 | 0 | |
| 125287901 | 12528790 | 4 | 20150218 | 201505 | 0 | |
| 125287901 | 12528790 | 5 | 20141125 | 0 | ||
| 125287901 | 12528790 | 6 | 20150218 | 201505 | 0 | |
| 125287901 | 12528790 | 7 | 20141125 | 0 |