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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784078 | 5888600 | F | 4784078-1 | 20050528 | 20050602 | 20050930 | PER | US-GLAXOSMITHKLINE-A0560859A | GLAXOSMITHKLINE | 58 | YR | F | Y | 51.4 | KG | 20050929 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784078 | 1006469485 | PS | FLOVENT | 1 | RESPIRATORY (INHALATION) | 2PUFF PER DAY | 021433 | ||||
| 4784078 | 1006469486 | C | BUDESONIDE | 1 | |||||||
| 4784078 | 1006469487 | C | ALUPENT | 1 | |||||||
| 4784078 | 1006469488 | C | CLARITIN | 1 | |||||||
| 4784078 | 1006469489 | C | ALENDRONATE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4784078 | 1006469485 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4784078 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4784078 | CHEST DISCOMFORT |
| 4784078 | PNEUMONITIS |
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 |
|---|---|---|---|---|---|
| 4784078 | 1006469485 | 20050527 |