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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195452 | 6206059 | I | 5195452-6 | 20061221 | 20061230 | EXP | DE-ABBOTT-06P-062-0353819-00 | ABBOTT | 51 | YR | M | Y | 20061230 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195452 | 1007999509 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 5195452 | 1007999510 | SS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 5195452 | 1007999511 | C | METHOTREXATE SODIUM | 1 | |||||||
| 5195452 | 1007999512 | C | GLUCOCORTICOIDS | 2 | ORAL | ||||||
| 5195452 | 1007999513 | C | ANALGESICS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5195452 | 1007999509 | RHEUMATOID ARTHRITIS |
| 5195452 | 1007999511 | RHEUMATOID ARTHRITIS |
| 5195452 | 1007999512 | RHEUMATOID ARTHRITIS |
| 5195452 | 1007999513 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5195452 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5195452 | ARTHROPATHY |
| 5195452 | RETROPERITONEAL NEOPLASM |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |