Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016611 | 8317502 | I | 8016611-0 | 20111228 | 20111231 | EXP | BR-ABBOTT-11P-020-0887526-00 | ABBOTT | YR | M | Y | 95 | KG | 20111231 | CN | BRAZIL |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016611 | 1018419874 | PS | HUMIRA | 1 | SUBCUTANEOUS | NOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016611 | 1018419874 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016611 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8016611 | OSTEOARTHRITIS |
| 8016611 | ARTHROPATHY |
| 8016611 | INCORRECT DRUG ADMINISTRATION DURATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |