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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795045 | 6686846 | I | 5795045-3 | 20071101 | 20080311 | 20080630 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-14111496 | BRISTOL-MYERS SQUIBB COMPANY | 50 | YR | F | Y | 75 | KG | 20080630 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795045 | 1010110902 | PS | ORENCIA | 1 | |||||||
| 5795045 | 1010110903 | C | MEDROL | 1 | |||||||
| 5795045 | 1010110904 | C | METHOTREXATE | 1 | |||||||
| 5795045 | 1010110905 | C | LEXAPRO | 1 | |||||||
| 5795045 | 1010110906 | C | CALTRATE + D | 2 | |||||||
| 5795045 | 1010110907 | C | ACTONEL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5795045 | 1010110902 | RHEUMATOID ARTHRITIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5795045 | DRUG INEFFECTIVE |
| 5795045 | RED BLOOD CELL SEDIMENTATION RATE INCREASED |
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 |
|---|---|---|---|---|---|
| 5795045 | 1010110902 | 20071101 |