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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248798 | 8233315 | F | 8248798-9 | 20111025 | 20120327 | 20120331 | EXP | VE-ABBOTT-11P-178-0871122-00 | ABBOTT | 52 | YR | F | Y | 20120331 | CN | VENEZUELA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248798 | 1019282960 | SS | HUMIRA | 1 | |||||||
| 8248798 | 1019282959 | PS | HUMIRA | 1 | 40MG/0.8ML EVERY OTHER WEEK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8248798 | 1019282959 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8248798 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8248798 | NASOPHARYNGITIS |
| 8248798 | PHARYNGITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8248798 | 1019282959 | 20080528 | 20111017 |