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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127054461 | 12705446 | 1 | I | 20160823 | 20160901 | 20160901 | EXP | CA-ABBVIE-16K-028-1711173-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160901 | CN | CA | CM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127054461 | 12705446 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | UNKNOWN | 125057 | SOLUTION FOR INJECTION | ||||||||
| 127054461 | 12705446 | 2 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 127054461 | 12705446 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | EVERY 7 TO 10 DAYS | UNKNOWN | 0 | 1 | MG | |||||||
| 127054461 | 12705446 | 4 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 127054461 | 12705446 | 5 | C | VITAMIN B12 | CYANOCOBALAMIN | 1 | Other | 0 | |||||||||||
| 127054461 | 12705446 | 6 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127054461 | 12705446 | 1 | Product used for unknown indication |
| 127054461 | 12705446 | 2 | Rheumatoid arthritis |
| 127054461 | 12705446 | 3 | Rheumatoid arthritis |
| 127054461 | 12705446 | 4 | Product used for unknown indication |
| 127054461 | 12705446 | 5 | Product used for unknown indication |
| 127054461 | 12705446 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127054461 | 12705446 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127054461 | 12705446 | Drug ineffective | |
| 127054461 | 12705446 | Mobility decreased | |
| 127054461 | 12705446 | Nausea | |
| 127054461 | 12705446 | Pneumothorax | |
| 127054461 | 12705446 | Rheumatoid arthritis | |
| 127054461 | 12705446 | Spinal fracture |
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 |
|---|---|---|---|---|---|---|
| 127054461 | 12705446 | 1 | 2014 | 2015 | 0 | |
| 127054461 | 12705446 | 3 | 2011 | 0 |