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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106579223 | 10657922 | 3 | F | 20110119 | 20110527 | 20141217 | 20160902 | EXP | CA-UCBSA-026175 | UCB | 55.34 | YR | F | Y | 84.00000 | KG | 20160902 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106579223 | 10657922 | 1 | PS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Subcutaneous | 200 MG, EV 2 WEEKS(QOW) | 55549 | 125160 | 200 | MG | SOLUTION FOR INJECTION | QOW | |||||
| 106579223 | 10657922 | 2 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | 5 MG, WEEKLY (QW) | 0 | 5 | MG | /wk | |||||||
| 106579223 | 10657922 | 3 | C | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | 25 MG, WEEKLY (QW) | 0 | 25 | MG | /wk | |||||||
| 106579223 | 10657922 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | 10 MG, WEEKLY (QW) | 0 | 10 | MG | /wk | ||||||||
| 106579223 | 10657922 | 5 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Oral | 200 MG, ONCE DAILY (QD) | 0 | 200 | MG | QD | |||||||
| 106579223 | 10657922 | 6 | C | VOLTAREN | DICLOFENAC SODIUM | 1 | Oral | 75 MG, AS NEEDED (PRN) | 0 | 75 | MG | ||||||||
| 106579223 | 10657922 | 7 | C | EMTEC | 2 | Oral | 30 MG, AS NEEDED (PRN) | 0 | 30 | MG | |||||||||
| 106579223 | 10657922 | 8 | C | AVELOX | MOXIFLOXACIN HYDROCHLORIDE | 1 | Oral | 400 MG, ONCE DAILY (QD) | U | 0 | 400 | MG | QD | ||||||
| 106579223 | 10657922 | 9 | C | NASONEX | MOMETASONE FUROATE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106579223 | 10657922 | 1 | Rheumatoid arthritis |
| 106579223 | 10657922 | 2 | Rheumatoid arthritis |
| 106579223 | 10657922 | 3 | Rheumatoid arthritis |
| 106579223 | 10657922 | 5 | Rheumatoid arthritis |
| 106579223 | 10657922 | 6 | Rheumatoid arthritis |
| 106579223 | 10657922 | 7 | Rheumatoid arthritis |
| 106579223 | 10657922 | 8 | Sinusitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106579223 | 10657922 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106579223 | 10657922 | Arthralgia | |
| 106579223 | 10657922 | Cough | |
| 106579223 | 10657922 | Dyspnoea | |
| 106579223 | 10657922 | Fatigue | |
| 106579223 | 10657922 | Injection site pain | |
| 106579223 | 10657922 | Nasal congestion | |
| 106579223 | 10657922 | Neuralgia | |
| 106579223 | 10657922 | Rhinorrhoea | |
| 106579223 | 10657922 | Sinusitis |
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 |
|---|---|---|---|---|---|---|
| 106579223 | 10657922 | 1 | 20101222 | 0 | ||
| 106579223 | 10657922 | 2 | 200809 | 0 | ||
| 106579223 | 10657922 | 3 | 200809 | 20110303 | 0 | |
| 106579223 | 10657922 | 4 | 20110304 | 0 | ||
| 106579223 | 10657922 | 5 | 200711 | 20110304 | 0 | |
| 106579223 | 10657922 | 7 | 20101206 | 0 |