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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125349832 | 12534983 | 2 | F | 201606 | 20160801 | 20160707 | 20160802 | EXP | US-009507513-1607USA001368 | MERCK | 70.51 | YR | F | Y | 0.00000 | 20160802 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125349832 | 12534983 | 1 | PS | DULERA | FORMOTEROL FUMARATE DIHYDRATEMOMETASONE FUROATE | 1 | Respiratory (inhalation) | UNK | 22518 | PRESSURISED INHALATION, SUSPENSION | |||||||||
| 125349832 | 12534983 | 2 | SS | DULERA | FORMOTEROL FUMARATE DIHYDRATEMOMETASONE FUROATE | 1 | 22518 | PRESSURISED INHALATION, SUSPENSION | |||||||||||
| 125349832 | 12534983 | 3 | SS | PROVENTIL | ALBUTEROL | 1 | Respiratory (inhalation) | UNK | 0 | INHALATION POWDER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125349832 | 12534983 | 1 | Asthma |
| 125349832 | 12534983 | 2 | Prophylaxis against bronchospasm |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125349832 | 12534983 | DE |
| 125349832 | 12534983 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125349832 | 12534983 | Death |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |