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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330789 | 4112367 | F | 1 | 4330789-1 | 20040317 | 20040331 | EXP | USA040360584 | ELI LILLY AND COMPANY | 82 | YR | F | N | 34 | KG | 20040324 | MD | 20031223 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330789 | 1004757087 | PS | FORTEO | 1 | 20 UG/1 DAY | D | 21318 | ||||
| 4330789 | 1004766343 | SS | EVISTA | 1 | 60 MG/1 DAY | D | |||||
| 4330789 | 1004766344 | C | PREDNISONE | 1 | |||||||
| 4330789 | 1004766345 | C | BEXTRA | 1 | |||||||
| 4330789 | 1004766346 | C | CALCIUM | 2 | |||||||
| 4330789 | 1004766347 | C | MULTI-VITAMIN | 1 | |||||||
| 4330789 | 1004766348 | C | METHOTREXATE | 1 | |||||||
| 4330789 | 1004766349 | C | CALTRATE (CALCIUM CARBONATE) | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4330789 | 1004757087 | DECREASED ACTIVITY |
| 4330789 | 1004757087 | OSTEOPOROSIS |
| 4330789 | 1004757087 | RHEUMATOID ARTHRITIS |
| 4330789 | 1004766343 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4330789 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4330789 | CHRONIC OBSTRUCTIVE AIRWAYS DISEASE |
| 4330789 | RHEUMATOID LUNG |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4330789 | CSM |
| 4330789 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4330789 | 1004757087 | 20030602 |