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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8622977 | 8746193 | I | 8622977-0 | 20120823 | 20120827 | EXP | PHHY2012FR073268 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | F | Y | 20120827 | OT | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8622977 | 1020667876 | PS | FEMARA | 1 | ORAL | 2.5 MG, QD | 020726 | ||||
| 8622977 | 1020667877 | C | AVASTIN | 1 | 21 DAYS IN A MONTH |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8622977 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8622977 | SENSE OF OPPRESSION |
| 8622977 | DYSPNOEA |
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 |
|---|---|---|---|---|---|
| 8622977 | 1020667876 | 20120507 | 20120525 | 19 | DAY |
| 8622977 | 1020667877 | 20111101 |