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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112567078 | 11256707 | 8 | F | 201401 | 20160822 | 20150709 | 20160831 | PER | US-GLAXOSMITHKLINE-US2015GSK098459 | GLAXOSMITHKLINE | 54.06 | YR | F | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112567078 | 11256707 | 1 | PS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 90 UG, U | U | 4ZP7172 | 20983 | 90 | UG | OROMUCOSAL SPRAY | |||||
| 112567078 | 11256707 | 2 | SS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | UNK | U | UNKNOWN | 20983 | OROMUCOSAL SPRAY | ||||||||
| 112567078 | 11256707 | 3 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | 500 UG, U | U | 5ZP7616 | 0 | 500 | UG | INHALATION POWDER | |||||
| 112567078 | 11256707 | 4 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | U | 0 | INHALATION POWDER | ||||||||||
| 112567078 | 11256707 | 5 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK UNK, U | U | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112567078 | 11256707 | 1 | Chronic obstructive pulmonary disease |
| 112567078 | 11256707 | 2 | Emphysema |
| 112567078 | 11256707 | 3 | Chronic obstructive pulmonary disease |
| 112567078 | 11256707 | 4 | Emphysema |
| 112567078 | 11256707 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 112567078 | 11256707 | OT |
| 112567078 | 11256707 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112567078 | 11256707 | Condition aggravated | |
| 112567078 | 11256707 | Drug ineffective | |
| 112567078 | 11256707 | Dyspnoea | |
| 112567078 | 11256707 | Dyspnoea exertional | |
| 112567078 | 11256707 | Hospitalisation | |
| 112567078 | 11256707 | Influenza | |
| 112567078 | 11256707 | Lung infection | |
| 112567078 | 11256707 | Oxygen supplementation | |
| 112567078 | 11256707 | Pneumonia | |
| 112567078 | 11256707 | Respiratory failure | |
| 112567078 | 11256707 | Therapeutic response decreased |
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 |
|---|---|---|---|---|---|---|
| 112567078 | 11256707 | 1 | 2011 | 0 | ||
| 112567078 | 11256707 | 3 | 2014 | 0 |