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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120598594 | 12059859 | 4 | F | 201509 | 20160715 | 20160210 | 20160727 | EXP | CA-CONCORDIA PHARMACEUTICALS INC.-CO-PL-CA-2016-037 | CONCORDIA | 58.00 | YR | F | Y | 0.00000 | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120598594 | 12059859 | 1 | PS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Oral | Y | 9768 | 200 | MG | QD | |||||||
| 120598594 | 12059859 | 2 | C | NAPROXEN. | NAPROXEN | 1 | 0 | ||||||||||||
| 120598594 | 12059859 | 3 | C | TYLENOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 120598594 | 12059859 | 4 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 120598594 | 12059859 | 5 | C | XELJANZ | TOFACITINIB CITRATE | 1 | 0 | ||||||||||||
| 120598594 | 12059859 | 6 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120598594 | 12059859 | 1 | Rheumatoid arthritis |
| 120598594 | 12059859 | 2 | Rheumatoid arthritis |
| 120598594 | 12059859 | 3 | Rheumatoid arthritis |
| 120598594 | 12059859 | 4 | Rheumatoid arthritis |
| 120598594 | 12059859 | 5 | Rheumatoid arthritis |
| 120598594 | 12059859 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120598594 | 12059859 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120598594 | 12059859 | Arthralgia | |
| 120598594 | 12059859 | Diarrhoea | |
| 120598594 | 12059859 | Drug effect incomplete | |
| 120598594 | 12059859 | Haemorrhage | |
| 120598594 | 12059859 | Herpes zoster | |
| 120598594 | 12059859 | Hypoaesthesia | |
| 120598594 | 12059859 | Joint lock | |
| 120598594 | 12059859 | Joint swelling | |
| 120598594 | 12059859 | Mobility decreased | |
| 120598594 | 12059859 | Peripheral swelling |
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 |
|---|---|---|---|---|---|---|
| 120598594 | 12059859 | 1 | 201503 | 0 | ||
| 120598594 | 12059859 | 5 | 20151118 | 0 | ||
| 120598594 | 12059859 | 6 | 201406 | 0 |