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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118019306 | 11801930 | 6 | F | 20160803 | 20151204 | 20160804 | EXP | CA-PFIZER INC-2015411810 | PFIZER | 71.00 | YR | F | Y | 0.00000 | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118019306 | 11801930 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | 0 | ||||||||||
| 118019306 | 11801930 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, WEEKLY | 11719 | 25 | MG | SOLUTION FOR INJECTION | /wk | ||||||
| 118019306 | 11801930 | 3 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | 500 MG X 2, UNK | 7073 | 500 | MG | |||||||||
| 118019306 | 11801930 | 4 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | 1 G, 2X/DAY | 7073 | 1 | G | BID | ||||||||
| 118019306 | 11801930 | 5 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | 500 MG X 2, UNK | 7073 | 500 | MG | |||||||||
| 118019306 | 11801930 | 6 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | UNK | U | 0 | ||||||||||
| 118019306 | 11801930 | 7 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 118019306 | 11801930 | 8 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118019306 | 11801930 | 1 | Rheumatoid arthritis |
| 118019306 | 11801930 | 2 | Rheumatoid arthritis |
| 118019306 | 11801930 | 3 | Rheumatoid arthritis |
| 118019306 | 11801930 | 6 | Rheumatoid arthritis |
| 118019306 | 11801930 | 7 | Rheumatoid arthritis |
| 118019306 | 11801930 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118019306 | 11801930 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118019306 | 11801930 | Drug intolerance | |
| 118019306 | 11801930 | Dyspepsia | |
| 118019306 | 11801930 | Nausea | |
| 118019306 | 11801930 | Thrombosis | |
| 118019306 | 11801930 | Treatment failure |
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 |
|---|---|---|---|---|---|---|
| 118019306 | 11801930 | 8 | 2012 | 201309 | 0 |