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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5795043 | 6686845 | I | 5795043-X | 20080310 | 20080311 | 20080630 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-14110860 | BRISTOL-MYERS SQUIBB COMPANY | 56 | YR | F | Y | 82 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5795043 | 1010110892 | PS | ORENCIA | 1 | |||||||
5795043 | 1010110893 | C | COZAAR | 1 | |||||||
5795043 | 1010110894 | C | VYTORIN | 1 | |||||||
5795043 | 1010110895 | C | DITROPAN | 1 | |||||||
5795043 | 1010110896 | C | PRILOSEC | 1 | |||||||
5795043 | 1010110897 | C | METHOTREXATE | 1 | |||||||
5795043 | 1010110898 | C | PREDNISONE | 1 | |||||||
5795043 | 1010110899 | C | VALIUM | 1 | |||||||
5795043 | 1010110900 | C | IBUROFEN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5795043 | 1010110892 | RHEUMATOID ARTHRITIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5795043 | INFLUENZA LIKE ILLNESS |
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 |
---|---|---|---|---|---|
5795043 | 1010110892 | 20080305 |