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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127194012 | 12719401 | 2 | F | 20160905 | 20160907 | 20160926 | PER | US-ASTRAZENECA-2016SE81654 | ASTRAZENECA | 0.00 | F | Y | 0.00000 | 20160926 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127194012 | 12719401 | 1 | PS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 180 MCG, 1-2 PUFFS ONCE OR TWICE PER DAY | U | U | PAKH | 20929 | INHALATION POWDER | ||||||
127194012 | 12719401 | 2 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 180 MCG, 1-2 PUFFS ONCE OR TWICE PER DAY | U | U | PAKH | 20929 | INHALATION POWDER |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127194012 | 12719401 | 1 | Bronchitis |
127194012 | 12719401 | 2 | Chronic obstructive pulmonary disease |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127194012 | 12719401 | Device issue | |
127194012 | 12719401 | Fatigue | |
127194012 | 12719401 | Hypersomnia | |
127194012 | 12719401 | Intentional product misuse | |
127194012 | 12719401 | Malaise | |
127194012 | 12719401 | Memory impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |