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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120628593 | 12062859 | 3 | F | 20151125 | 20160829 | 20160210 | 20160908 | EXP | CA-PFIZER INC-2016073292 | PFIZER | 29.00 | YR | F | Y | 0.00000 | 20160908 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120628593 | 12062859 | 1 | PS | SULFASALAZINE. | SULFASALAZINE | 1 | 1000 MG, 2X/DAY | Y | 7073 | 1000 | MG | BID | |||||||
| 120628593 | 12062859 | 2 | C | HUMIRA | ADALIMUMAB | 1 | 40 MG, WEEKLY (40MG/0.8ML) | 0 | 40 | MG | /wk | ||||||||
| 120628593 | 12062859 | 3 | C | HYDROXYCHLOROQUINE SULFATE. | HYDROXYCHLOROQUINE SULFATE | 1 | Oral | 400 MG, 1X/DAY 200MG TABLET; 2 TABLETS DAILY | 0 | 400 | MG | QD | |||||||
| 120628593 | 12062859 | 4 | C | ARAVA | LEFLUNOMIDE | 1 | 20 MG, DAILY | 0 | 20 | MG | TABLET | ||||||||
| 120628593 | 12062859 | 5 | C | FERROUS GLUCONATE | FERROUS GLUCONATE | 1 | 600 MG, ALTERNATE DAY ((35 MG IRON) ORAL TABLET [600 MG EVERY TWO DAYS)) | 0 | 600 | MG | TABLET | QOD | |||||||
| 120628593 | 12062859 | 6 | C | LAMOTRIGINE. | LAMOTRIGINE | 1 | Oral | 100 MG, UNK | 0 | 100 | MG | TABLET | |||||||
| 120628593 | 12062859 | 7 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 400 MG, DAILY | 0 | 400 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120628593 | 12062859 | 1 | Rheumatoid arthritis |
| 120628593 | 12062859 | 2 | Rheumatoid arthritis |
| 120628593 | 12062859 | 3 | Rheumatoid arthritis |
| 120628593 | 12062859 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120628593 | 12062859 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120628593 | 12062859 | Back pain | |
| 120628593 | 12062859 | Drug intolerance | |
| 120628593 | 12062859 | Joint swelling | |
| 120628593 | 12062859 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 120628593 | 12062859 | 1 | 20151125 | 201512 | 0 |