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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127953131 | 12795313 | 1 | I | 2015 | 20160924 | 20160929 | 20160929 | PER | US-GLAXOSMITHKLINE-US2016GSK142073 | GLAXOSMITHKLINE | 65.00 | YR | Y | 0.00000 | 20160929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127953131 | 12795313 | 1 | PS | FLOVENT | FLUTICASONE PROPIONATE | 1 | U | 21433 | |||||||||||
| 127953131 | 12795313 | 2 | SS | FLOVENT | FLUTICASONE PROPIONATE | 1 | U | 21433 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127953131 | 12795313 | 1 | Bronchitis chronic |
| 127953131 | 12795313 | 2 | Cough |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127953131 | 12795313 | Aphonia | |
| 127953131 | 12795313 | Cough | |
| 127953131 | 12795313 | Upper respiratory tract infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |