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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120067053 | 12006705 | 3 | F | 20160125 | 20160804 | 20160204 | 20160818 | EXP | US-GLAXOSMITHKLINE-US2016009917 | GLAXOSMITHKLINE | 62.22 | YR | F | Y | 0.00000 | 20160818 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120067053 | 12006705 | 1 | PS | FLOVENT DISKUS | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | 2 PUFF(S), BID | MJ7Y | 21433 | 2 | DF | BID | ||||||
120067053 | 12006705 | 2 | SS | FLOVENT DISKUS | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | 2 PUFF(S), BID | MV3N | 21433 | 2 | DF | BID | ||||||
120067053 | 12006705 | 3 | SS | FLOVENT DISKUS | FLUTICASONE PROPIONATE | 1 | UNK, 2, PUFFS QAM AND 1 PUFF QPM | 21433 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
120067053 | 12006705 | 1 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
120067053 | 12006705 | Device use error | |
120067053 | 12006705 | Product quality issue | |
120067053 | 12006705 | Underdose |
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 |
---|---|---|---|---|---|---|
120067053 | 12006705 | 1 | 2015 | 0 |