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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119334944 | 11933494 | 4 | F | 20120822 | 20160810 | 20160121 | 20160815 | EXP | CA-ROCHE-1135497 | ROCHE | 49.58 | YR | F | Y | 82.63000 | KG | 20160815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119334944 | 11933494 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | 125276 | 664 | MG | SOLUTION FOR INFUSION | /month | |||||||
| 119334944 | 11933494 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | 125276 | 600 | MG | SOLUTION FOR INFUSION | ||||||||
| 119334944 | 11933494 | 3 | SS | VOLTAREN | DICLOFENAC SODIUM | 1 | Unknown | 0 | |||||||||||
| 119334944 | 11933494 | 4 | C | ARTHROTEC | DICLOFENAC SODIUMMISOPROSTOL | 1 | 0 | ||||||||||||
| 119334944 | 11933494 | 5 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 | ||||||||||||
| 119334944 | 11933494 | 6 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 | ||||||||||||
| 119334944 | 11933494 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 119334944 | 11933494 | 8 | C | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 119334944 | 11933494 | 9 | C | Rabeprazole | RABEPRAZOLE | 1 | 0 | ||||||||||||
| 119334944 | 11933494 | 10 | C | NORVASC | AMLODIPINE BESYLATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119334944 | 11933494 | 1 | Rheumatoid arthritis |
| 119334944 | 11933494 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119334944 | 11933494 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119334944 | 11933494 | Abdominal pain upper | |
| 119334944 | 11933494 | Arthralgia | |
| 119334944 | 11933494 | Back pain | |
| 119334944 | 11933494 | Blood pressure increased | |
| 119334944 | 11933494 | Chest pain | |
| 119334944 | 11933494 | Drug ineffective | |
| 119334944 | 11933494 | Hypertension | |
| 119334944 | 11933494 | Joint lock | |
| 119334944 | 11933494 | Musculoskeletal pain | |
| 119334944 | 11933494 | Nausea | |
| 119334944 | 11933494 | Neck pain | |
| 119334944 | 11933494 | Pain in extremity | |
| 119334944 | 11933494 | Therapeutic response decreased | |
| 119334944 | 11933494 | Vomiting | |
| 119334944 | 11933494 | Weight 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 |
|---|---|---|---|---|---|---|
| 119334944 | 11933494 | 1 | 20120822 | 0 | ||
| 119334944 | 11933494 | 2 | 20130416 | 0 | ||
| 119334944 | 11933494 | 3 | 2014 | 0 |