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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126926091 | 12692609 | 1 | I | 2015 | 20160816 | 20160829 | 20160829 | PER | US-ASTRAZENECA-2016SE89024 | ASTRAZENECA | 4.00 | YR | F | Y | 22.70000 | KG | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126926091 | 12692609 | 1 | PS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 UG, ONE PUFF DAILY IN THE MORNING | U | U | BACM | 21949 | INHALATION POWDER | ||||||
126926091 | 12692609 | 2 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 UG, ONE PUFF DAILY IN THE MORNING | U | U | BACM | 21949 | INHALATION POWDER | ||||||
126926091 | 12692609 | 3 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 UG, IF HAVING AN ALLERGY FLAREUP, 2 PUFFS IN THE MORNING | U | U | BACM | 21949 | INHALATION POWDER | ||||||
126926091 | 12692609 | 4 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 UG, IF HAVING AN ALLERGY FLAREUP, 2 PUFFS IN THE MORNING | U | U | BACM | 21949 | INHALATION POWDER | ||||||
126926091 | 12692609 | 5 | C | FLONASE | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | TOOK 1 PUFF OF FLONASE IN EACH NOSTRIL | 0 | ||||||||||
126926091 | 12692609 | 6 | C | CLARITIN | LORATADINE | 1 | Oral | DAILY AS NEEDED | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126926091 | 12692609 | 1 | Hypersensitivity |
126926091 | 12692609 | 2 | Ill-defined disorder |
126926091 | 12692609 | 3 | Hypersensitivity |
126926091 | 12692609 | 4 | Ill-defined disorder |
126926091 | 12692609 | 5 | Multiple allergies |
126926091 | 12692609 | 6 | Multiple allergies |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126926091 | 12692609 | Cough | |
126926091 | 12692609 | Drug dose omission | |
126926091 | 12692609 | Off label use | |
126926091 | 12692609 | Product quality issue | |
126926091 | 12692609 | Product use 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 |
---|---|---|---|---|---|---|
126926091 | 12692609 | 1 | 2015 | 0 | ||
126926091 | 12692609 | 2 | 2015 | 0 | ||
126926091 | 12692609 | 3 | 2015 | 0 | ||
126926091 | 12692609 | 4 | 2015 | 0 |