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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124065632 | 12406563 | 2 | F | 2008 | 20160708 | 20160526 | 20160715 | EXP | US-ASTRAZENECA-2016SE54300 | ASTRAZENECA | 59.00 | YR | F | Y | 136.10000 | KG | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124065632 | 12406563 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG, 2 PUFFS TWICE A DAY | U | U | 21929 | Q12H | |||||||
| 124065632 | 12406563 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | ONLY TOOK IN THE MORNING, DAILY | U | U | 21929 | QD | |||||||
| 124065632 | 12406563 | 3 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 0 | 5 | MG | QD | ||||||||
| 124065632 | 12406563 | 4 | C | XOPENEX | LEVALBUTEROL HYDROCHLORIDE | 1 | Respiratory (inhalation) | AS REQUIRED | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124065632 | 12406563 | 1 | Chronic obstructive pulmonary disease |
| 124065632 | 12406563 | 2 | Chronic obstructive pulmonary disease |
| 124065632 | 12406563 | 3 | Chronic obstructive pulmonary disease |
| 124065632 | 12406563 | 4 | Chronic obstructive pulmonary disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124065632 | 12406563 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124065632 | 12406563 | Device malfunction | |
| 124065632 | 12406563 | Dysphonia | |
| 124065632 | 12406563 | Dyspnoea | |
| 124065632 | 12406563 | Intentional product misuse | |
| 124065632 | 12406563 | Multiple organ dysfunction syndrome |
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 |
|---|---|---|---|---|---|---|
| 124065632 | 12406563 | 1 | 2008 | 0 |