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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127248961 | 12724896 | 1 | I | 20160823 | 20160908 | 20160908 | PER | US-ASTRAZENECA-2016SE91336 | ASTRAZENECA | 0.00 | F | Y | 56.70000 | KG | 20160908 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127248961 | 12724896 | 1 | PS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 180 MCG 225 MG, 1 PUFF DAILY | PAKM,PAKD | 21949 | INHALATION POWDER | ||||||||
| 127248961 | 12724896 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | U | 0 | ||||||||||
| 127248961 | 12724896 | 3 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | Oral | 0 | 10 | MG | QD | ||||||||
| 127248961 | 12724896 | 4 | C | ALBUTEROL. | ALBUTEROL | 1 | Respiratory (inhalation) | 2 PUFFS,15 MINUTES BEFORE SHE RUNS | 0 | ||||||||||
| 127248961 | 12724896 | 5 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | Oral | 0 | 40 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127248961 | 12724896 | 1 | Asthma |
| 127248961 | 12724896 | 2 | Asthma |
| 127248961 | 12724896 | 3 | Asthma |
| 127248961 | 12724896 | 4 | Exercise test abnormal |
| 127248961 | 12724896 | 5 | Gastrooesophageal reflux disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127248961 | 12724896 | Drug dose omission | |
| 127248961 | 12724896 | Intentional product misuse | |
| 127248961 | 12724896 | Malaise | |
| 127248961 | 12724896 | Off label use | |
| 127248961 | 12724896 | Product quality issue |
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 |
|---|---|---|---|---|---|---|
| 127248961 | 12724896 | 2 | 2009 | 201212 | 0 | |
| 127248961 | 12724896 | 3 | 2007 | 0 |