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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125082622 | 12508262 | 2 | F | 20160628 | 20160629 | 20160701 | EXP | US-GLAXOSMITHKLINE-US2016092607 | GLAXOSMITHKLINE | 0.00 | M | Y | 0.00000 | 20160701 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125082622 | 12508262 | 1 | PS | FLONASE | FLUTICASONE PROPIONATE | 1 | UNK UNK, BID | Y | K5087 | 205434 | NASAL SPRAY | BID | |||||||
125082622 | 12508262 | 2 | SS | FLONASE | FLUTICASONE PROPIONATE | 1 | UNK UNK, BID | Y | H5079 | 205434 | NASAL SPRAY | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125082622 | 12508262 | 1 | Hypersensitivity |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125082622 | 12508262 | Erythema | |
125082622 | 12508262 | Nasal discomfort |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |