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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123986452 | 12398645 | 2 | F | 20160817 | 20160524 | 20160826 | EXP | CA-PFIZER INC-2016251953 | PFIZER | 0.00 | M | Y | 0.00000 | 20160826 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123986452 | 12398645 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | U | 0 | ||||||||||
| 123986452 | 12398645 | 2 | PS | IBUPROFEN. | IBUPROFEN | 1 | UNK | U | 18989 | ||||||||||
| 123986452 | 12398645 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | UNK | U | 0 | ||||||||||
| 123986452 | 12398645 | 4 | SS | NAPROSYN | NAPROXEN | 1 | UNK | U | 0 | ||||||||||
| 123986452 | 12398645 | 5 | SS | ORENCIA | ABATACEPT | 1 | UNK | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123986452 | 12398645 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123986452 | 12398645 | Drug ineffective | |
| 123986452 | 12398645 | Impaired work ability |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |