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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125473521 | 12547352 | 1 | I | 20160602 | 20160711 | 20160711 | PER | US-APOTEX-2016AP008943 | APOTEX | 0.00 | M | Y | 88.89000 | KG | 20160711 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125473521 | 12547352 | 1 | PS | FLUTICASONE PROPIONATE NASAL SPRAY USP | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | UNK | MT8406 | 77538 | NASAL SPRAY, SUSPENSION | ||||||||
125473521 | 12547352 | 2 | SS | FLUTICASONE PROPIONATE NASAL SPRAY USP | FLUTICASONE PROPIONATE | 1 | 77538 | NASAL SPRAY, SUSPENSION | |||||||||||
125473521 | 12547352 | 3 | SS | FLUTICASONE PROPIONATE NASAL SPRAY USP | FLUTICASONE PROPIONATE | 1 | 77538 | NASAL SPRAY, SUSPENSION | |||||||||||
125473521 | 12547352 | 4 | SS | FLUTICASONE PROPIONATE NASAL SPRAY USP | FLUTICASONE PROPIONATE | 1 | 77538 | NASAL SPRAY, SUSPENSION | |||||||||||
125473521 | 12547352 | 5 | C | GLIPIZIDE. | GLIPIZIDE | 1 | Unknown | UNK | U | U | 0 | ||||||||
125473521 | 12547352 | 6 | C | METOPROLOL. | METOPROLOL | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125473521 | 12547352 | 1 | Nasal congestion |
125473521 | 12547352 | 2 | Rhinorrhoea |
125473521 | 12547352 | 3 | Eye pruritus |
125473521 | 12547352 | 4 | Sneezing |
125473521 | 12547352 | 5 | Product used for unknown indication |
125473521 | 12547352 | 6 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125473521 | 12547352 | Drug ineffective |
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 |
---|---|---|---|---|---|---|
125473521 | 12547352 | 1 | 20160601 | 0 |