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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122548413 | 12254841 | 3 | F | 20151224 | 20160803 | 20160411 | 20160815 | EXP | US-TEVA-649869USA | TEVA | 82.12 | YR | F | Y | 54.48000 | KG | 20160815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122548413 | 12254841 | 1 | PS | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | TWO INHALATIONS EVERY FOUR TO SIX HOURS | Y | UNKNOWN | 21457 | ||||||||
| 122548413 | 12254841 | 2 | SS | ANORO ELLIPTA | UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE | 1 | Respiratory (inhalation) | U | 0 | ||||||||||
| 122548413 | 12254841 | 3 | C | FLOVENT HFA | FLUTICASONE PROPIONATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122548413 | 12254841 | 1 | Asthma |
| 122548413 | 12254841 | 3 | Asthma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122548413 | 12254841 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122548413 | 12254841 | Dysphonia | |
| 122548413 | 12254841 | Dyspnoea | |
| 122548413 | 12254841 | Pneumonia | |
| 122548413 | 12254841 | Throat irritation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |