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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5795556 | 6687188 | I | 5795556-0 | 20080619 | 20080630 | EXP | PHHY2008JP12014 | NOVARTIS PHARMACEUTICALS CORP. | 26 | YR | M | Y | 20080630 | PH | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5795556 | 1010112663 | PS | ZADITEN | 1 | ORAL | UNK | 021066 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5795556 | 1010112663 | RHINORRHOEA |
Outcome of event
Event ID | OUTC COD |
---|---|
5795556 | OT |
Reactions reported
Event ID | PT |
---|---|
5795556 | ACCIDENTAL OVERDOSE |
5795556 | SOMNOLENCE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |