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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6767569 | 7362796 | F | 6767569-3 | 20100404 | 20100601 | 20100614 | EXP | PHHY2010FR22953 | NOVARTIS PHARMACEUTICAL CORPORATION | 72 | YR | F | Y | 59 | KG | 20100614 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6767569 | 1013857271 | PS | RASILEZ | 2 | ORAL | 300 MG, QD | 21985 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6767569 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6767569 | ERYTHEMA |
| 6767569 | EYELID OEDEMA |
| 6767569 | HEADACHE |
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 |
|---|---|---|---|---|---|
| 6767569 | 1013857271 | 20100329 | 20100408 | 11 | DAY |