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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126851831 | 12685183 | 1 | I | 2016 | 20160818 | 20160825 | 20160825 | EXP | AT-UCBSA-2016032278 | UCB | 63.00 | YR | F | Y | 65.00000 | KG | 20160825 | MD | AT | AT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126851831 | 12685183 | 1 | PS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Subcutaneous | 200 MG, EV 2 WEEKS(QOW) | Y | U | 125160 | 200 | MG | SOLUTION FOR INJECTION | QOW | ||||
126851831 | 12685183 | 2 | C | ORENCIA | ABATACEPT | 1 | UNK | U | 0 | ||||||||||
126851831 | 12685183 | 3 | C | Etx | ETORICOXIB | 1 | 10 MG, WEEKLY (QW) | Y | U | 0 | 10 | MG | /wk | ||||||
126851831 | 12685183 | 4 | C | Aprednislon | PREDNISOLONE | 1 | UNK | U | 0 | ||||||||||
126851831 | 12685183 | 5 | C | Aprednislon | PREDNISOLONE | 1 | 5 MG, ONCE DAILY (QD) | U | 0 | 5 | MG | QD | |||||||
126851831 | 12685183 | 6 | C | Imurek | AZATHIOPRINE | 1 | 50 MG, ONCE DAILY (QD) | U | 0 | 50 | MG | QD | |||||||
126851831 | 12685183 | 7 | C | SIMPONI | GOLIMUMAB | 1 | Subcutaneous | 50 MG, MONTHLY (QM) | U | 0 | 50 | MG | /month |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126851831 | 12685183 | 1 | Crohn's disease |
126851831 | 12685183 | 2 | Product used for unknown indication |
126851831 | 12685183 | 3 | Product used for unknown indication |
126851831 | 12685183 | 4 | Product used for unknown indication |
126851831 | 12685183 | 6 | Product used for unknown indication |
126851831 | 12685183 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126851831 | 12685183 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126851831 | 12685183 | Diarrhoea haemorrhagic | |
126851831 | 12685183 | Pneumonia | |
126851831 | 12685183 | Synovial disorder |
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 |
---|---|---|---|---|---|---|
126851831 | 12685183 | 1 | 201602 | 201603 | 0 | |
126851831 | 12685183 | 4 | 201603 | 2016 | 0 | |
126851831 | 12685183 | 5 | 201607 | 0 |