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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4387434 | 4161874 | F | 4387434-9 | 20040201 | 20040216 | 20040630 | PER | US-GLAXOSMITHKLINE-A0507543A | GLAXOSMITHKLINE | 65 | YR | M | Y | 20040630 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4387434 | 1004978927 | PS | ADVAIR HFA | 1 | RESPIRATORY (INHALATION) | 1PUFF TWICE PER DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4387434 | 1004978927 | ASTHMA |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 4387434 | DRUG INEFFECTIVE |
| 4387434 | DYSPNOEA |
| 4387434 | PHARMACEUTICAL PRODUCT COMPLAINT |
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 |
|---|---|---|---|---|---|
| 4387434 | 1004978927 | 2 |