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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125067442 | 12506744 | 2 | F | 20160624 | 20160628 | 20160818 | PER | US-ASTRAZENECA-2016SE57096 | ASTRAZENECA | 0.00 | F | Y | 0.00000 | 20160819 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125067442 | 12506744 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG 120 INHALATIONS, TWO TIMES A DAY | 21929 | BID | |||||||||
125067442 | 12506744 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG 120 INHALATIONS, TWO TIMES A DAY | 21929 | BID | |||||||||
125067442 | 12506744 | 3 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG 120 INHALATIONS, TWO TIMES A DAY | 3001181C00 | 21929 | BID | ||||||||
125067442 | 12506744 | 4 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160/4.5 MCG 120 INHALATIONS, TWO TIMES A DAY | 3001181C00 | 21929 | BID | ||||||||
125067442 | 12506744 | 5 | C | XOPENEX | LEVALBUTEROL HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125067442 | 12506744 | 1 | Asthma |
125067442 | 12506744 | 2 | Chronic obstructive pulmonary disease |
125067442 | 12506744 | 3 | Asthma |
125067442 | 12506744 | 4 | Chronic obstructive pulmonary disease |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125067442 | 12506744 | Device malfunction | |
125067442 | 12506744 | Fatigue | |
125067442 | 12506744 | Off label use of device | |
125067442 | 12506744 | Pulmonary function test decreased |
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 |
---|---|---|---|---|---|---|
125067442 | 12506744 | 1 | 201602 | 0 | ||
125067442 | 12506744 | 2 | 201602 | 0 | ||
125067442 | 12506744 | 3 | 2016 | 0 | ||
125067442 | 12506744 | 4 | 2016 | 0 |