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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128000701 | 12800070 | 1 | I | 20160926 | 20160930 | 20160930 | PER | US-GLAXOSMITHKLINE-US2016142757 | GLAXOSMITHKLINE | 0.00 | Y | 0.00000 | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128000701 | 12800070 | 1 | PS | FLONASE | FLUTICASONE PROPIONATE | 1 | UNK | U | UNK | 205434 | NASAL SPRAY | ||||||||
| 128000701 | 12800070 | 2 | SS | FLONASE | FLUTICASONE PROPIONATE | 1 | U | 205434 | NASAL SPRAY | ||||||||||
| 128000701 | 12800070 | 3 | SS | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | UNK | U | UNK | 0 | |||||||||
| 128000701 | 12800070 | 4 | SS | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 128000701 | 12800070 | 1 | Rhinorrhoea |
| 128000701 | 12800070 | 2 | Hypersensitivity |
| 128000701 | 12800070 | 3 | Hypersensitivity |
| 128000701 | 12800070 | 4 | Rhinorrhoea |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 128000701 | 12800070 | Dyspnoea | |
| 128000701 | 12800070 | Nasal congestion |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |