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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195451 | 6192086 | F | 5195451-4 | 20061211 | 20061230 | EXP | DE-ABBOTT-06P-062-0353156-00 | ABBOTT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195451 | 1007999505 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 5195451 | 1007999506 | SS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 5195451 | 1007999507 | C | METHOTREXATE SODIUM | 1 | |||||||
| 5195451 | 1007999508 | C | HEART MEDS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5195451 | 1007999505 | RHEUMATOID ARTHRITIS |
| 5195451 | 1007999507 | RHEUMATOID ARTHRITIS |
| 5195451 | 1007999508 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5195451 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5195451 | CARDIAC PACEMAKER INSERTION |
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 |
|---|---|---|---|---|---|
| 5195451 | 1007999505 | 20060401 | |||
| 5195451 | 1007999507 | 20020901 |