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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120884982 | 12088498 | 2 | F | 20160912 | 20160218 | 20160915 | EXP | CA-ROCHE-1710070 | ROCHE | 66.00 | YR | M | Y | 0.00000 | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120884982 | 12088498 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | U | 125276 | ||||||||||
| 120884982 | 12088498 | 2 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 120884982 | 12088498 | 3 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | U | 0 | ||||||||||
| 120884982 | 12088498 | 4 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | U | 0 | ||||||||||
| 120884982 | 12088498 | 5 | C | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | 0 | 25 | MG | |||||||||
| 120884982 | 12088498 | 6 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 | |||||||||||
| 120884982 | 12088498 | 7 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | 0 | 200 | MG | BID | ||||||||
| 120884982 | 12088498 | 8 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Unknown | 0 | 40 | MG | QD | ||||||||
| 120884982 | 12088498 | 9 | C | GABAPENTIN. | GABAPENTIN | 1 | 0 | ||||||||||||
| 120884982 | 12088498 | 10 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 0 | 1 | DF | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120884982 | 12088498 | 1 | Rheumatoid arthritis |
| 120884982 | 12088498 | 2 | Rheumatoid arthritis |
| 120884982 | 12088498 | 3 | Rheumatoid arthritis |
| 120884982 | 12088498 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120884982 | 12088498 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120884982 | 12088498 | Arthritis | |
| 120884982 | 12088498 | Condition aggravated | |
| 120884982 | 12088498 | Nuclear magnetic resonance imaging abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |