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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075894 | 6102561 | I | 5075894-X | 20060225 | 20060802 | 20060809 | EXP | FI-BRISTOL-MYERS SQUIBB COMPANY-13463013 | BRISTOL-MYERS SQUIBB COMPANY | 65 | YR | F | Y | 20060809 | OT | FINLAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075894 | 1007561415 | PS | TREXAN (ORION) | 2 | ORAL | 86358 | |||||
| 5075894 | 1007561416 | SS | PREDNISONE | 1 | ORAL | ||||||
| 5075894 | 1007561417 | SS | HUMIRA | 1 | SUBCUTANEOUS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5075894 | 1007561415 | RHEUMATOID ARTHRITIS |
| 5075894 | 1007561416 | RHEUMATOID ARTHRITIS |
| 5075894 | 1007561417 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5075894 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5075894 | LYMPH NODE TUBERCULOSIS |
| 5075894 | PULMONARY TUBERCULOSIS |
| 5075894 | TUBERCULOUS PLEURISY |
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 |
|---|---|---|---|---|---|
| 5075894 | 1007561417 | 20041129 |