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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126010622 | 12601062 | 2 | F | 20160804 | 20160728 | 20160816 | EXP | CA-ABBVIE-16K-028-1684651-00 | ABBVIE | 58.00 | YR | F | Y | 0.00000 | 20160816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126010622 | 12601062 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | N | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION | ||||||
| 126010622 | 12601062 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | U | UNKNOWN | 0 | 20 | MG | /wk | ||||||
| 126010622 | 12601062 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Oral | U | UNKNOWN | 0 | |||||||||
| 126010622 | 12601062 | 4 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | 20MG/DAY | UNKNOWN | 0 | 20 | MG | QD | ||||||
| 126010622 | 12601062 | 5 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | UNKNOWN | 0 | 1500 | MG | BID | |||||||
| 126010622 | 12601062 | 6 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNKNOWN | 0 | 400 | MG | QD | |||||||
| 126010622 | 12601062 | 7 | C | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 126010622 | 12601062 | 8 | C | RAMIPRIL. | RAMIPRIL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126010622 | 12601062 | 1 | Rheumatoid arthritis |
| 126010622 | 12601062 | 2 | Rheumatoid arthritis |
| 126010622 | 12601062 | 3 | Rheumatoid arthritis |
| 126010622 | 12601062 | 4 | Rheumatoid arthritis |
| 126010622 | 12601062 | 5 | Rheumatoid arthritis |
| 126010622 | 12601062 | 6 | Product used for unknown indication |
| 126010622 | 12601062 | 7 | Pain |
| 126010622 | 12601062 | 8 | Blood pressure measurement |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126010622 | 12601062 | DS |
| 126010622 | 12601062 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126010622 | 12601062 | Drug ineffective | |
| 126010622 | 12601062 | Hand deformity | |
| 126010622 | 12601062 | Joint arthroplasty | |
| 126010622 | 12601062 | Knee arthroplasty | |
| 126010622 | 12601062 | Mobility decreased | |
| 126010622 | 12601062 | Pain | |
| 126010622 | 12601062 | 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 |
|---|---|---|---|---|---|---|
| 126010622 | 12601062 | 1 | 20150924 | 20160714 | 0 | |
| 126010622 | 12601062 | 2 | 2005 | 2015 | 0 | |
| 126010622 | 12601062 | 4 | 20120913 | 0 | ||
| 126010622 | 12601062 | 5 | 2005 | 0 | ||
| 126010622 | 12601062 | 6 | 2005 | 0 |