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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112217717 | 11221771 | 7 | F | 2015 | 20160809 | 20150626 | 20160817 | EXP | CA-PFIZER INC-2015104261 | PFIZER | 54.00 | YR | F | Y | 0.00000 | 20160817 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112217717 | 11221771 | 1 | PS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | Y | 203214 | 5 | MG | TABLET | BID | |||||
| 112217717 | 11221771 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | UNK | 11719 | SOLUTION FOR INJECTION | ||||||||||
| 112217717 | 11221771 | 3 | SS | CELEBREX | CELECOXIB | 1 | Oral | UNK | 20998 | CAPSULE, HARD | |||||||||
| 112217717 | 11221771 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | 0 | |||||||||||
| 112217717 | 11221771 | 5 | C | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112217717 | 11221771 | 1 | Rheumatoid arthritis |
| 112217717 | 11221771 | 2 | Rheumatoid arthritis |
| 112217717 | 11221771 | 3 | Rheumatoid arthritis |
| 112217717 | 11221771 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 112217717 | 11221771 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112217717 | 11221771 | Back pain | |
| 112217717 | 11221771 | Bone erosion | |
| 112217717 | 11221771 | Condition aggravated | |
| 112217717 | 11221771 | Fatigue | |
| 112217717 | 11221771 | Inflammation | |
| 112217717 | 11221771 | Lower respiratory tract infection | |
| 112217717 | 11221771 | Memory impairment | |
| 112217717 | 11221771 | Musculoskeletal pain | |
| 112217717 | 11221771 | Plantar fasciitis | |
| 112217717 | 11221771 | Rheumatoid arthritis | |
| 112217717 | 11221771 | Sciatica | |
| 112217717 | 11221771 | Tendon rupture | |
| 112217717 | 11221771 | Tendonitis |
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 |
|---|---|---|---|---|---|---|
| 112217717 | 11221771 | 1 | 20141001 | 20160629 | 0 |