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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113596073 | 11359607 | 3 | F | 20160320 | 20160610 | 20150807 | 20160822 | PER | US-ASTRAZENECA-2015SE73801 | ASTRAZENECA | 24225.00 | DY | F | Y | 0.00000 | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113596073 | 11359607 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 2 PUFFS TWICE A DAY | 3001028C00 | 21929 | |||||||||
| 113596073 | 11359607 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 2 PUFFS TWICE A DAY | 3001028C00 | 21929 | |||||||||
| 113596073 | 11359607 | 3 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 20 MG PO DAILY FOR 3 YEARS | 0 | ||||||||||
| 113596073 | 11359607 | 4 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 20 MG PO DAILY FOR 3 YEARS | 0 | ||||||||||
| 113596073 | 11359607 | 5 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 1000 IU PO | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 113596073 | 11359607 | 1 | Chronic obstructive pulmonary disease |
| 113596073 | 11359607 | 2 | Bronchiectasis |
| 113596073 | 11359607 | 5 | Supplementation therapy |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 113596073 | 11359607 | Cough | |
| 113596073 | 11359607 | Intentional product use issue | |
| 113596073 | 11359607 | Oral mucosal erythema | |
| 113596073 | 11359607 | Product quality issue | |
| 113596073 | 11359607 | Rash pruritic |
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 |
|---|---|---|---|---|---|---|
| 113596073 | 11359607 | 1 | 20160607 | 0 | ||
| 113596073 | 11359607 | 2 | 20160607 | 0 | ||
| 113596073 | 11359607 | 4 | 201603 | 20160610 | 0 | |
| 113596073 | 11359607 | 5 | 20160608 | 0 |