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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330797 | 4041630 | F | 1 | 4330797-0 | 20040311 | 20040331 | EXP | USA031152405 | ELI LILLY AND COMPANY | F | N | 76 | KG | 20040324 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330797 | 1004757106 | PS | EVISTA | 1 | 60 MG | 20815 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4330797 | HO |
| 4330797 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4330797 | BLOOD CHOLESTEROL INCREASED |
| 4330797 | CEREBROVASCULAR ACCIDENT |
| 4330797 | CONDITION AGGRAVATED |
| 4330797 | HYPOTENSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4330797 | CR |
| 4330797 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4330797 | 1004757106 | 6 | WK |