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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040799 | 6080046 | I | 5040799-7 | 20060629 | 20060630 | DIR | 73 | YR | F | N | 125 | LBS | 20060629 | N | N | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040799 | 1007433099 | PS | FLUTICASONE PROPIONATE | 1 | NASAL | 2 SPRAYS IN EACH NOSTRIL ONCE DAILY NASAL | Y | Y | C224781 | 20080229 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5040799 | 1007433099 | HYPERSENSITIVITY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5040799 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5040799 | COUGH |
| 5040799 | EPISTAXIS |
| 5040799 | NASAL DRYNESS |
| 5040799 | PHARMACEUTICAL PRODUCT COMPLAINT |
| 5040799 | THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION |
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 |
|---|---|---|---|---|---|
| 5040799 | 1007433099 | 20060606 | 20060622 | 16 | DAY |