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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4919808 | 5930477 | F | 1 | 4919808-9 | 20050318 | 20060131 | 20060216 | EXP | JP_051108108 | ELI LILLY AND COMPANY | 76 | YR | F | N | 20060208 | OT | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4919808 | 1006965059 | PS | EVISTA | 1 | ORAL | 60 MG, DAILY (1/D), ORAL | Y | D | 20815 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4919808 | 1006965059 | OSTEOPOROSIS POSTMENOPAUSAL |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4919808 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4919808 | GASTRITIS HAEMORRHAGIC |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4919808 | FGN |
| 4919808 | HP |
| 4919808 | OTH |
| 4919808 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4919808 | 1006965059 | 20050225 | 20050318 |