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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122482952 | 12248295 | 2 | F | 20160329 | 20160830 | 20160408 | 20160906 | EXP | US-ASTRAZENECA-2016SE36367 | ASTRAZENECA | 26383.00 | DY | M | Y | 77.10000 | KG | 20160906 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122482952 | 12248295 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5MCG 2 PUFFS TWICE DAILY | 21929 | BID | |||||||||
| 122482952 | 12248295 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5MCG 2 PUFFS TWICE DAILY | 3001138C00 | 21929 | BID | ||||||||
| 122482952 | 12248295 | 3 | C | DUONEB | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | Respiratory (inhalation) | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122482952 | 12248295 | 1 | Chronic obstructive pulmonary disease |
| 122482952 | 12248295 | 2 | Chronic obstructive pulmonary disease |
| 122482952 | 12248295 | 3 | Chronic obstructive pulmonary disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122482952 | 12248295 | HO |
| 122482952 | 12248295 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122482952 | 12248295 | Atrial fibrillation | |
| 122482952 | 12248295 | Blindness unilateral | |
| 122482952 | 12248295 | Choking | |
| 122482952 | 12248295 | Cough | |
| 122482952 | 12248295 | Foreign body | |
| 122482952 | 12248295 | Intentional device misuse | |
| 122482952 | 12248295 | Pneumonia | |
| 122482952 | 12248295 | Product quality issue |
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 |
|---|---|---|---|---|---|---|
| 122482952 | 12248295 | 2 | 201603 | 0 |