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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126663341 | 12666334 | 1 | I | 20160810 | 20160818 | 20160818 | EXP | NL-ASTRAZENECA-2016SE88022 | ASTRAZENECA | 0.00 | F | Y | 0.00000 | 20160818 | NL | NL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126663341 | 12666334 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | U | 21929 | INHALATION POWDER | |||||||||
126663341 | 12666334 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | U | 21929 | INHALATION POWDER | |||||||||
126663341 | 12666334 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | U | 21929 | INHALATION POWDER |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126663341 | 12666334 | 1 | Chronic obstructive pulmonary disease |
126663341 | 12666334 | 2 | Asthma |
126663341 | 12666334 | 3 | Lower respiratory tract infection fungal |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126663341 | 12666334 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126663341 | 12666334 | Balance disorder | |
126663341 | 12666334 | Fall | |
126663341 | 12666334 | Wrist fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |