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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127220652 | 12722065 | 2 | F | 20160919 | 20160907 | 20160922 | PER | US-GLAXOSMITHKLINE-US2016129283 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160922 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127220652 | 12722065 | 1 | PS | FLONASE | FLUTICASONE PROPIONATE | 1 | UNK | Y | UNK | 205434 | NASAL SPRAY | ||||||||
| 127220652 | 12722065 | 2 | SS | FLONASE | FLUTICASONE PROPIONATE | 1 | Y | 205434 | NASAL SPRAY | ||||||||||
| 127220652 | 12722065 | 3 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | UNK, EVERY 2-3 HOURS | Y | UNK | 0 | |||||||||
| 127220652 | 12722065 | 4 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127220652 | 12722065 | 1 | Multiple allergies |
| 127220652 | 12722065 | 2 | Dyspnoea |
| 127220652 | 12722065 | 3 | Multiple allergies |
| 127220652 | 12722065 | 4 | Dyspnoea |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127220652 | 12722065 | Hypertension | |
| 127220652 | 12722065 | Hypotension | |
| 127220652 | 12722065 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |