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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126872611 | 12687261 | 1 | I | 20160817 | 20160825 | 20160825 | PER | US-GLAXOSMITHKLINE-US2016120362 | GLAXOSMITHKLINE | 0.00 | A | F | Y | 0.00000 | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126872611 | 12687261 | 1 | PS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 500/50 MCG, 1 PUFF(S), BID | N | UNKNOWN | 21077 | 1 | DF | INHALATION POWDER | BID | |||||
| 126872611 | 12687261 | 2 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 250/50 MCG, UNK | N | UNKNOWN | 21077 | INHALATION POWDER | ||||||||
| 126872611 | 12687261 | 3 | SS | PROAIR HFA | ALBUTEROL SULFATE | 1 | UNK UNK, Z (9 TIMES PER DAY PER PATIENT) | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126872611 | 12687261 | 1 | Asthma |
| 126872611 | 12687261 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126872611 | 12687261 | Intentional product misuse | |
| 126872611 | 12687261 | Overdose | |
| 126872611 | 12687261 | Palpitations |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |