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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124578662 | 12457866 | 2 | F | 20160123 | 20160628 | 20160612 | 20160705 | EXP | US-UCBSA-2016021517 | UCB | 40.88 | YR | F | Y | 145.00000 | KG | 20160705 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124578662 | 12457866 | 1 | PS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Subcutaneous | 400 MG, EV 4 WEEKS | Y | 125160 | 400 | MG | SOLUTION FOR INJECTION | ||||||
| 124578662 | 12457866 | 2 | C | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | MG, ONCE DAILY (QD) | U | 0 | QD | ||||||||
| 124578662 | 12457866 | 3 | C | CELEBREX | CELECOXIB | 1 | Oral | MG, ONCE DAILY (QD) | U | 0 | QD | ||||||||
| 124578662 | 12457866 | 4 | C | TRAMADOL. | TRAMADOL | 1 | Oral | MG, AS NEEDED (PRN) | U | 0 | |||||||||
| 124578662 | 12457866 | 5 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 60 MG, ON/OFF (AS PRESCRIBED FOR ASTHMA) | U | 0 | 60 | MG | |||||||
| 124578662 | 12457866 | 6 | C | METHOTREXATE. | METHOTREXATE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124578662 | 12457866 | 1 | Rheumatoid arthritis |
| 124578662 | 12457866 | 2 | Crohn's disease |
| 124578662 | 12457866 | 3 | Rheumatoid arthritis |
| 124578662 | 12457866 | 4 | Rheumatoid arthritis |
| 124578662 | 12457866 | 5 | Asthma |
| 124578662 | 12457866 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124578662 | 12457866 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124578662 | 12457866 | Nausea | |
| 124578662 | 12457866 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 124578662 | 12457866 | 1 | 201601 | 2016 | 0 |