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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127875211 | 12787521 | 1 | I | 201604 | 20160923 | 20160928 | 20160928 | PER | US-GLAXOSMITHKLINE-US2016139914 | GLAXOSMITHKLINE | 48.88 | YR | F | Y | 0.00000 | 20160928 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127875211 | 12787521 | 1 | PS | FLOVENT DISKUS | FLUTICASONE PROPIONATE | 1 | Oral | 2 PUFF(S), BID | UB2C | 21433 | 2 | DF | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127875211 | 12787521 | 1 | Eosinophilic oesophagitis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127875211 | 12787521 | Drug ineffective | |
127875211 | 12787521 | Off label use | |
127875211 | 12787521 | Product cleaning inadequate | |
127875211 | 12787521 | Therapeutic response unexpected |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
127875211 | 12787521 | 1 | 201604 | 0 |