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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126204032 | 12620403 | 2 | F | 20160518 | 20160810 | 20160803 | 20160828 | PER | US-ASTRAZENECA-2016SE71087 | ASTRAZENECA | 0.00 | F | Y | 0.00000 | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126204032 | 12620403 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80-4.5MCG, TWO PUFFS TWICE A DAY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80-4.5MCG, TWO PUFFS TWICE A DAY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80-4.5MCG, TWO PUFFS TWICE A DAY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 4 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80-4.5MCG, TWO PUFFS TWICE A DAY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 5 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | ONE PUFF, DAILY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 6 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | ONE PUFF, DAILY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 7 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | ONE PUFF, DAILY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 8 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | ONE PUFF, DAILY | U | U | 21929 | ||||||||
| 126204032 | 12620403 | 9 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | 0 | ||||||||||||
| 126204032 | 12620403 | 10 | C | BRIO | 2 | 0 | |||||||||||||
| 126204032 | 12620403 | 11 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126204032 | 12620403 | 1 | Bronchitis |
| 126204032 | 12620403 | 2 | Sinusitis |
| 126204032 | 12620403 | 3 | Wheezing |
| 126204032 | 12620403 | 4 | Chronic obstructive pulmonary disease |
| 126204032 | 12620403 | 5 | Bronchitis |
| 126204032 | 12620403 | 6 | Sinusitis |
| 126204032 | 12620403 | 7 | Wheezing |
| 126204032 | 12620403 | 8 | Chronic obstructive pulmonary disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126204032 | 12620403 | Drug dose omission | |
| 126204032 | 12620403 | Drug ineffective | |
| 126204032 | 12620403 | Dysphonia | |
| 126204032 | 12620403 | Dyspnoea | |
| 126204032 | 12620403 | Heart rate increased | |
| 126204032 | 12620403 | Intentional product misuse | |
| 126204032 | 12620403 | Nausea | |
| 126204032 | 12620403 | Off label use | |
| 126204032 | 12620403 | Product use issue | |
| 126204032 | 12620403 | Sinus disorder |
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 |
|---|---|---|---|---|---|---|
| 126204032 | 12620403 | 1 | 20160518 | 201605 | 0 | |
| 126204032 | 12620403 | 2 | 20160518 | 201605 | 0 | |
| 126204032 | 12620403 | 3 | 20160518 | 201605 | 0 | |
| 126204032 | 12620403 | 4 | 20160518 | 201605 | 0 | |
| 126204032 | 12620403 | 10 | 201605 | 0 |