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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127329441 | 12732944 | 1 | I | 20160905 | 0 | 20160911 | 20160911 | DIR | US-FDA-350326 | FDA-CTU | 33.00 | YR | M | N | 76.50000 | KG | 20160911 | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127329441 | 12732944 | 1 | PS | FLONASE | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | OTHER STRENGTH:MCG;OTHER DOSE:;OTHER FREQUENCY:;OTHER ROUTE: | N | D | E6925 | 20180501 | 0 | 2 | UG/M**2 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127329441 | 12732944 | 1 | Multiple allergies |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127329441 | 12732944 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127329441 | 12732944 | Anxiety | |
| 127329441 | 12732944 | Depression | |
| 127329441 | 12732944 | Feeling abnormal | |
| 127329441 | 12732944 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 127329441 | 12732944 | 1 | 20160824 | 20160909 | 0 |