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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127371121 | 12737112 | 1 | I | 20160830 | 20160912 | 20160912 | PER | US-ASTRAZENECA-2016SE92881 | ASTRAZENECA | 8.00 | YR | M | Y | 0.00000 | 20160912 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127371121 | 12737112 | 1 | PS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90MCG ONE PUFF TWICE DAILY | 20929 | INHALATION POWDER | |||||||||
127371121 | 12737112 | 2 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90MCG ONE PUFF TWICE DAILY | 20929 | INHALATION POWDER | |||||||||
127371121 | 12737112 | 3 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 MCG 2 PUFFS TWICE A DAY. | 20929 | INHALATION POWDER | |||||||||
127371121 | 12737112 | 4 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 MCG 2 PUFFS TWICE A DAY. | 20929 | INHALATION POWDER |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127371121 | 12737112 | 1 | Asthma |
127371121 | 12737112 | 2 | Hypersensitivity |
127371121 | 12737112 | 3 | Asthma |
127371121 | 12737112 | 4 | Hypersensitivity |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127371121 | 12737112 | Candida infection | |
127371121 | 12737112 | Drug administered to patient of inappropriate age | |
127371121 | 12737112 | Intentional product misuse | |
127371121 | 12737112 | Off label use | |
127371121 | 12737112 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |