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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195433 | 6172419 | F | 5195433-2 | 20061113 | 20061230 | EXP | SE-NOVOPROD-258666 | NOVOPROD | 59 | YR | F | Y | 62.7 | KG | 20061230 | MD | SWEDEN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195433 | 1007999394 | PS | ACTIVELLE | 1 | ORAL | .25 MG, QD | 020907 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5195433 | 1007999394 | MENOPAUSAL SYMPTOMS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5195433 | HO |
| 5195433 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5195433 | BREAST CANCER |
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 |
|---|---|---|---|---|---|
| 5195433 | 1007999394 | 20040929 | 20050531 | 244 | DAY |