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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122533552 | 12253355 | 2 | F | 20160629 | 20160411 | 20160706 | EXP | CA-PFIZER INC-2016195801 | PFIZER | 57.00 | YR | F | Y | 0.00000 | 20160706 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122533552 | 12253355 | 1 | PS | CELEBREX | CELECOXIB | 1 | Oral | UNK, 1X/DAY | 20998 | CAPSULE, HARD | QD | ||||||||
| 122533552 | 12253355 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | UNK | 11719 | |||||||||||
| 122533552 | 12253355 | 3 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | QD | |||||||
| 122533552 | 12253355 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | 40MG/''0.0ML'' | 0 | |||||||||||
| 122533552 | 12253355 | 5 | SS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | 200MG/ML ''X2'' | 0 | |||||||||||
| 122533552 | 12253355 | 6 | SS | ARAVA | LEFLUNOMIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122533552 | 12253355 | 1 | Rheumatoid arthritis |
| 122533552 | 12253355 | 2 | Rheumatoid arthritis |
| 122533552 | 12253355 | 3 | Rheumatoid arthritis |
| 122533552 | 12253355 | 4 | Rheumatoid arthritis |
| 122533552 | 12253355 | 5 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122533552 | 12253355 | HO |
| 122533552 | 12253355 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122533552 | 12253355 | Blood pressure decreased | |
| 122533552 | 12253355 | Diarrhoea | |
| 122533552 | 12253355 | Drug ineffective | |
| 122533552 | 12253355 | Loss of consciousness | |
| 122533552 | 12253355 | Lupus-like syndrome |
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 |
|---|---|---|---|---|---|---|
| 122533552 | 12253355 | 3 | 20121129 | 20150625 | 0 | |
| 122533552 | 12253355 | 4 | 20121127 | 20131127 | 0 | |
| 122533552 | 12253355 | 5 | 20131107 | 20141107 | 0 | |
| 122533552 | 12253355 | 6 | 20160324 | 0 |