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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5526850 | 6475482 | I | 5526850-6 | 20071001 | 20071120 | 20071127 | EXP | FR-ASTRAZENECA-2007CG01651 | AZPRODUW00 | M | Y | 20071127 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5526850 | 1009197957 | PS | RHINOCORT | 1 | NASAL | 020746 | |||||
5526850 | 1009197958 | C | TAHOR | 2 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5526850 | HO |
Reactions reported
Event ID | PT |
---|---|
5526850 | STRABISMUS |
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 |
---|---|---|---|---|---|
5526850 | 1009197957 | 20020101 |