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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127760311 | 12776031 | 1 | I | 20160907 | 20160913 | 20160923 | 20160923 | EXP | US-TEVA-693262USA | TEVA | 73.76 | YR | F | Y | 88.53000 | KG | 20160923 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127760311 | 12776031 | 1 | PS | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | D | DAA23A | 21457 | |||||||||
| 127760311 | 12776031 | 2 | SS | PROAIR HFA | ALBUTEROL SULFATE | 1 | D | DAA23A | 21457 | ||||||||||
| 127760311 | 12776031 | 3 | SS | ALBUTEROL. | ALBUTEROL | 1 | Respiratory (inhalation) | D | 77772 | NEBULISER SOLUTION | |||||||||
| 127760311 | 12776031 | 4 | SS | BUDESONIDE. | BUDESONIDE | 1 | Respiratory (inhalation) | D | 77519 | NEBULISER SOLUTION | |||||||||
| 127760311 | 12776031 | 5 | C | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127760311 | 12776031 | 1 | Chronic obstructive pulmonary disease |
| 127760311 | 12776031 | 2 | Dyspnoea |
| 127760311 | 12776031 | 3 | Asthma |
| 127760311 | 12776031 | 5 | Chronic obstructive pulmonary disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127760311 | 12776031 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127760311 | 12776031 | Chest pain | |
| 127760311 | 12776031 | Dyspnoea | |
| 127760311 | 12776031 | Product use issue | |
| 127760311 | 12776031 | Pulmonary function test decreased |
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 |
|---|---|---|---|---|---|---|
| 127760311 | 12776031 | 1 | 2006 | 0 | ||
| 127760311 | 12776031 | 5 | 2006 | 0 |