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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6137763 | 6956400 | I | 6137763-3 | 20090323 | 20090331 | EXP | US-ASTRAZENECA-2009UW07364 | AZPRODUW00 | 46 | YR | F | Y | 20090331 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6137763 | 1011355043 | PS | ARIMIDEX | 1 | ORAL | 020541 | |||||
| 6137763 | 1011355044 | C | CYMBALTA | 1 | |||||||
| 6137763 | 1011355045 | C | NORTRIPTYLINE HCL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6137763 | 1011355043 | BREAST CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6137763 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6137763 | DEPRESSION |
| 6137763 | MENTAL STATUS CHANGES |
| 6137763 | SUICIDAL IDEATION |
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 |
|---|---|---|---|---|---|
| 6137763 | 1011355043 | 25 | DAY |