Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105686493 | 10568649 | 3 | F | 20160728 | 20141106 | 20160815 | EXP | US-GLAXOSMITHKLINE-US2014GSK016699 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160815 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105686493 | 10568649 | 1 | PS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK | U | UNKNOWN | 21077 | INHALATION POWDER | ||||||||
| 105686493 | 10568649 | 2 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK | U | 3ZP2341 | 21077 | INHALATION POWDER | ||||||||
| 105686493 | 10568649 | 3 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK | U | 5ZP2436 | 21077 | INHALATION POWDER | ||||||||
| 105686493 | 10568649 | 4 | SS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | UNK | U | 0 | ||||||||||
| 105686493 | 10568649 | 5 | SS | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | U | 4ZP6329 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 105686493 | 10568649 | 1 | Chronic obstructive pulmonary disease |
| 105686493 | 10568649 | 2 | Emphysema |
| 105686493 | 10568649 | 3 | Asthma |
| 105686493 | 10568649 | 4 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105686493 | 10568649 | Dyspnoea | |
| 105686493 | 10568649 | Dyspnoea exertional | |
| 105686493 | 10568649 | Hypersensitivity | |
| 105686493 | 10568649 | Incorrect dosage administered | |
| 105686493 | 10568649 | Pruritus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 105686493 | 10568649 | 1 | 2011 | 0 |