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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125218293 | 12521829 | 3 | F | 2016 | 20160719 | 20160701 | 20160726 | EXP | US-UCBSA-2016024606 | UCB | 63.08 | YR | F | Y | 66.00000 | KG | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125218293 | 12521829 | 1 | PS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Subcutaneous | 400 MG, EV 2 WEEKS(QOW) | N | 125160 | 400 | MG | SOLUTION FOR INJECTION | QOW | |||||
| 125218293 | 12521829 | 2 | C | KEFLEX | CEPHALEXIN | 1 | UNK | U | 0 | ||||||||||
| 125218293 | 12521829 | 3 | C | Atorvastatin | ATORVASTATIN | 1 | Oral | 40 MG, ONCE DAILY (QD) | U | 0 | 40 | MG | QD | ||||||
| 125218293 | 12521829 | 4 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 40 MG, ONCE DAILY (QD) | U | 0 | 40 | MG | QD | ||||||
| 125218293 | 12521829 | 5 | C | BACTRIM | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | 800MG-160 MG, 2X/DAY (BID) | U | 0 | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125218293 | 12521829 | 1 | Rheumatoid arthritis |
| 125218293 | 12521829 | 2 | Post procedural infection |
| 125218293 | 12521829 | 3 | Blood cholesterol |
| 125218293 | 12521829 | 4 | Gastric disorder |
| 125218293 | 12521829 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125218293 | 12521829 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125218293 | 12521829 | Nausea | |
| 125218293 | 12521829 | Post procedural infection |
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 |
|---|---|---|---|---|---|---|
| 125218293 | 12521829 | 1 | 20160616 | 20160616 | 0 | |
| 125218293 | 12521829 | 2 | 2016 | 2016 | 0 | |
| 125218293 | 12521829 | 5 | 2016 | 0 |