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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126800012 | 12680001 | 2 | F | 201606 | 20160818 | 20160824 | 20160831 | EXP | US-CELGENEUS-USA-2016085287 | CELGENE | 60.31 | YR | F | Y | 0.00000 | 20160831 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126800012 | 12680001 | 1 | PS | OTEZLA | APREMILAST | 1 | Oral | 60 MILLIGRAM | U | VA9055840 | 205437 | 30 | MG | TABLETS | BID | ||||
| 126800012 | 12680001 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | U | 0 | UNKNOWN | ||||||||
| 126800012 | 12680001 | 3 | SS | ISONIAZID. | ISONIAZID | 1 | Unknown | U | U | 0 | UNKNOWN | ||||||||
| 126800012 | 12680001 | 4 | SS | Atorvastatin | ATORVASTATIN | 1 | Unknown | U | U | 0 | UNKNOWN | ||||||||
| 126800012 | 12680001 | 5 | SS | FOLIC ACID. | FOLIC ACID | 1 | Unknown | U | U | 0 | UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126800012 | 12680001 | 1 | Psoriatic arthropathy |
| 126800012 | 12680001 | 2 | Psoriatic arthropathy |
| 126800012 | 12680001 | 3 | Bacterial infection |
| 126800012 | 12680001 | 4 | Prophylaxis |
| 126800012 | 12680001 | 5 | Supplementation therapy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126800012 | 12680001 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126800012 | 12680001 | Decreased appetite | |
| 126800012 | 12680001 | Dizziness | |
| 126800012 | 12680001 | Feeling abnormal | |
| 126800012 | 12680001 | Headache | |
| 126800012 | 12680001 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 126800012 | 12680001 | 1 | 20160501 | 0 | ||
| 126800012 | 12680001 | 2 | 20160516 | 0 | ||
| 126800012 | 12680001 | 3 | 20160516 | 0 | ||
| 126800012 | 12680001 | 4 | 20160516 | 0 | ||
| 126800012 | 12680001 | 5 | 20160516 | 0 |