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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124569662 | 12456966 | 2 | F | 20160712 | 20160610 | 20160722 | EXP | US-GLAXOSMITHKLINE-US2016076044 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160722 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124569662 | 12456966 | 1 | PS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | UNK, PRN | U | 5ZP1648 | 20983 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124569662 | 12456966 | 1 | Asthma |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124569662 | 12456966 | Device use error | |
| 124569662 | 12456966 | Drug ineffective | |
| 124569662 | 12456966 | Dysphonia | |
| 124569662 | 12456966 | Dyspnoea | |
| 124569662 | 12456966 | Malaise | |
| 124569662 | 12456966 | Product cleaning inadequate | |
| 124569662 | 12456966 | Product quality issue | |
| 124569662 | 12456966 | Speech disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |