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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 86709793 | 8670979 | 3 | F | 2015 | 20160429 | 20120718 | 20160823 | PER | US-ASTRAZENECA-2012SE43583 | ASTRAZENECA | 59.00 | YR | F | Y | 63.50000 | KG | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 86709793 | 8670979 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 2 PUFFS, TWO TIMES A DAY | UNKNOWN | 21929 | |||||||||
| 86709793 | 8670979 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 2 PUFFS TWO TIMES A DAY | UNKNOWN | 21929 | |||||||||
| 86709793 | 8670979 | 3 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 0 | 10 | MG | QD | ||||||||
| 86709793 | 8670979 | 4 | C | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | AS REQUIRED | 0 | ||||||||||
| 86709793 | 8670979 | 5 | C | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | AS REQUIRED | 0 | ||||||||||
| 86709793 | 8670979 | 6 | C | MULTIVITAMIN | VITAMINS | 1 | Oral | 0 | 1 | DF | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 86709793 | 8670979 | 1 | Chronic obstructive pulmonary disease |
| 86709793 | 8670979 | 2 | Chronic obstructive pulmonary disease |
| 86709793 | 8670979 | 3 | Rheumatoid arthritis |
| 86709793 | 8670979 | 4 | Dyspnoea |
| 86709793 | 8670979 | 5 | Wheezing |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 86709793 | 8670979 | Accident | |
| 86709793 | 8670979 | Arthralgia | |
| 86709793 | 8670979 | Device failure | |
| 86709793 | 8670979 | Dyspnoea | |
| 86709793 | 8670979 | Exercise tolerance decreased | |
| 86709793 | 8670979 | Fall | |
| 86709793 | 8670979 | Fatigue | |
| 86709793 | 8670979 | Hypersensitivity | |
| 86709793 | 8670979 | Intentional product misuse | |
| 86709793 | 8670979 | Rheumatoid arthritis | |
| 86709793 | 8670979 | Seasonal allergy | |
| 86709793 | 8670979 | Sinus disorder | |
| 86709793 | 8670979 | Wheezing |
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 |
|---|---|---|---|---|---|---|
| 86709793 | 8670979 | 2 | 20160410 | 0 | ||
| 86709793 | 8670979 | 3 | 201603 | 0 |