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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4387179 | 4161619 | F | 4387179-5 | 20030901 | 20040318 | 20040630 | PER | US-GLAXOSMITHKLINE-A0503712A | GLAXOSMITHKLINE | 15 | YR | F | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4387179 | 1004978282 | PS | ADVAIR HFA | 1 | RESPIRATORY (INHALATION) | 1PUFF TWICE PER DAY | |||||
| 4387179 | 1004978283 | C | SINGULAIR | 1 | 10MG PER DAY | ||||||
| 4387179 | 1004978284 | C | ALLEGRA | 1 | 180MG PER DAY | ||||||
| 4387179 | 1004978285 | C | ALBUTEROL | 1 | |||||||
| 4387179 | 1004978286 | C | FLOVENT | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4387179 | 1004978282 | ASTHMA |
| 4387179 | 1004978283 | DRUG USE FOR UNKNOWN INDICATION |
| 4387179 | 1004978284 | DRUG USE FOR UNKNOWN INDICATION |
| 4387179 | 1004978285 | DRUG USE FOR UNKNOWN INDICATION |
| 4387179 | 1004978286 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 4387179 | WEIGHT INCREASED |
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 |
|---|---|---|---|---|---|
| 4387179 | 1004978282 | 20030714 |