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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127337891 | 12733789 | 1 | I | 20151105 | 20160912 | 20160912 | EXP | CA-ROCHE-1657747 | ROCHE | 50.00 | YR | M | Y | 0.00000 | 20160912 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127337891 | 12733789 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | MOST RECENT DOSE:14/OCT/2015 | 125276 | ||||||||||
| 127337891 | 12733789 | 2 | SS | ARAVA | LEFLUNOMIDE | 1 | Oral | PILL | U | 0 | 10 | MG | TABLET | QD | |||||
| 127337891 | 12733789 | 3 | SS | FOLIC ACID. | FOLIC ACID | 1 | Oral | 1 PILL/WEEK | U | 0 | 5 | MG | TABLET | /wk | |||||
| 127337891 | 12733789 | 4 | SS | PREDNISONE. | PREDNISONE | 1 | Oral | PREDNISONE 15 DAILY TIMES THREE DAYS | U | 0 | 5 | MG | TABLET | ||||||
| 127337891 | 12733789 | 5 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | U | 0 | 2.5 | MG | TABLET | /wk | ||||||
| 127337891 | 12733789 | 6 | C | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | 0 | 5 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127337891 | 12733789 | 1 | Rheumatoid arthritis |
| 127337891 | 12733789 | 2 | Rheumatoid arthritis |
| 127337891 | 12733789 | 3 | Rheumatoid arthritis |
| 127337891 | 12733789 | 4 | Rheumatoid arthritis |
| 127337891 | 12733789 | 5 | Rheumatoid arthritis |
| 127337891 | 12733789 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127337891 | 12733789 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127337891 | 12733789 | Activities of daily living impaired | |
| 127337891 | 12733789 | Arthralgia | |
| 127337891 | 12733789 | Blood pressure increased | |
| 127337891 | 12733789 | Condition aggravated | |
| 127337891 | 12733789 | Foot deformity | |
| 127337891 | 12733789 | Haemoglobin decreased | |
| 127337891 | 12733789 | Joint swelling | |
| 127337891 | 12733789 | Oropharyngeal pain | |
| 127337891 | 12733789 | Red cell distribution width increased | |
| 127337891 | 12733789 | Therapeutic response decreased |
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 |
|---|---|---|---|---|---|---|
| 127337891 | 12733789 | 2 | 20151115 | 0 | ||
| 127337891 | 12733789 | 6 | 20151029 | 0 |