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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4784334 | 5888832 | I | 4784334-7 | 20050922 | 20050930 | EXP | PHBS2005NZ13931 | NOVARTIS PHARMACEUTICALS CORP. | 15 | YR | F | Y | 20050929 | MD | NEW ZEALAND |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4784334 | 1006470459 | PS | ZASTEN | 2 | ORAL | 10 MG/DAY | 21066 | ||||
4784334 | 1006470460 | C | BUDESONIDE | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4784334 | OT |
Reactions reported
Event ID | PT |
---|---|
4784334 | ANGIONEUROTIC OEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |