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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119648776 | 11964877 | 6 | F | 20150813 | 20160816 | 20160127 | 20160819 | EXP | CA-ROCHE-1621866 | ROCHE | 72.09 | YR | F | Y | 79.00000 | KG | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119648776 | 11964877 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | Y | B2033B20,B2035 | 125276 | 635 | MG | SOLUTION FOR INFUSION | ||||||
| 119648776 | 11964877 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Subcutaneous | 125472 | 162 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||||
| 119648776 | 11964877 | 3 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119648776 | 11964877 | 1 | Rheumatoid arthritis |
| 119648776 | 11964877 | 2 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119648776 | 11964877 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119648776 | 11964877 | Anxiety | |
| 119648776 | 11964877 | Arthralgia | |
| 119648776 | 11964877 | Blood pressure increased | |
| 119648776 | 11964877 | Depression | |
| 119648776 | 11964877 | Headache | |
| 119648776 | 11964877 | Heart rate decreased | |
| 119648776 | 11964877 | Insomnia | |
| 119648776 | 11964877 | Rheumatoid arthritis | |
| 119648776 | 11964877 | Urticaria | |
| 119648776 | 11964877 | Weight decreased | |
| 119648776 | 11964877 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 119648776 | 11964877 | 1 | 20150813 | 20151229 | 0 | |
| 119648776 | 11964877 | 2 | 20160420 | 0 |