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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577638 | 6515741 | I | 5577638-1 | 20071212 | 20071219 | 20071231 | EXP | PHHO2007DE20749 | NOVARTIS PHARMACEUTICALS CORP. | 60 | YR | F | Y | 68 | KG | 20071229 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577638 | 1009349358 | SS | LETROZOLE | 1 | ORAL | 2.5 MG, QD | |||||
| 5577638 | 1009349359 | PS | ZOMETA | 1 | 021223 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577638 | 1009349358 | BREAST CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577638 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 5577638 | ARTHRITIS |
| 5577638 | ERYTHEMA |
| 5577638 | PAIN IN EXTREMITY |
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 |
|---|---|---|---|---|---|
| 5577638 | 1009349358 | 20071212 |