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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125303182 | 12530318 | 2 | F | 20160526 | 20160705 | 20160706 | 20160816 | PER | US-ASTRAZENECA-2016SE59708 | ASTRAZENECA | 23835.00 | DY | F | Y | 70.30000 | KG | 20160816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125303182 | 12530318 | 1 | PS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 180 MCG 225 MG,TWO TIMES A DAY | PAKW | 21949 | INHALATION POWDER | ||||||||
| 125303182 | 12530318 | 2 | C | OTC SINUS MEDICINE | 2 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125303182 | 12530318 | 1 | Asthma |
| 125303182 | 12530318 | 2 | Sinus disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125303182 | 12530318 | Chest discomfort | |
| 125303182 | 12530318 | Device issue | |
| 125303182 | 12530318 | Drug dose omission | |
| 125303182 | 12530318 | Intentional product misuse | |
| 125303182 | 12530318 | Product quality issue | |
| 125303182 | 12530318 | 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 |
|---|---|---|---|---|---|---|
| 125303182 | 12530318 | 1 | 20160515 | 0 |