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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195445 | 6130018 | F | 5195445-9 | 20050518 | 20060908 | 20061230 | EXP | DE-ABBOTT-06P-062-0343454-00 | ABBOTT | F | Y | 80 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195445 | 1007999474 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 5195445 | 1007999475 | C | AZATHIOPRINE | 1 | ORAL | ||||||
| 5195445 | 1007999476 | C | PREDNISOLONE | 1 | ORAL | ||||||
| 5195445 | 1007999477 | C | PHENPROCOUMON | 2 | |||||||
| 5195445 | 1007999478 | C | ERGOCALCIFEROL | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5195445 | 1007999474 | RHEUMATOID ARTHRITIS |
| 5195445 | 1007999475 | RHEUMATOID ARTHRITIS |
| 5195445 | 1007999476 | RHEUMATOID ARTHRITIS |
| 5195445 | 1007999477 | DRUG USE FOR UNKNOWN INDICATION |
| 5195445 | 1007999478 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5195445 | HO |
| 5195445 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 5195445 | PULMONARY EMBOLISM |
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 |
|---|---|---|---|---|---|
| 5195445 | 1007999474 | 20040527 | 20060801 | ||
| 5195445 | 1007999475 | 20030101 | 20060801 | ||
| 5195445 | 1007999477 | 20060501 |