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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121062622 | 12106262 | 2 | F | 2010 | 20160510 | 20160223 | 20160817 | PER | US-ASTRAZENECA-2016SE15063 | ASTRAZENECA | 41.00 | YR | F | Y | 56.70000 | KG | 20160817 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121062622 | 12106262 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 160 INTERMITTENT | U | U | UNKNOWN | 21929 | |||||||
121062622 | 12106262 | 2 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | U | 0 | 20 | MG | QD | |||||||
121062622 | 12106262 | 3 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | INTERMITTENT | 0 | ||||||||||
121062622 | 12106262 | 4 | C | MONOLUKEST SODIUM | 2 | Oral | 0 | 10 | MG | QD | |||||||||
121062622 | 12106262 | 5 | C | AZELASTINE HYDROCHLORIDE. | AZELASTINE HYDROCHLORIDE | 1 | Nasal | 2 UNK TWO TIMES A DAY | 0 | ||||||||||
121062622 | 12106262 | 6 | C | KETOTIFEN FUMURATE | 2 | INTERMITTENT | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121062622 | 12106262 | 1 | Asthma |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121062622 | 12106262 | Asthma | |
121062622 | 12106262 | Barrett's oesophagus | |
121062622 | 12106262 | Candida infection | |
121062622 | 12106262 | Coeliac disease | |
121062622 | 12106262 | Drug dose omission | |
121062622 | 12106262 | Dyspnoea | |
121062622 | 12106262 | Hiatus hernia | |
121062622 | 12106262 | Intentional product misuse | |
121062622 | 12106262 | Nasopharyngitis | |
121062622 | 12106262 | Vomiting |
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 |
---|---|---|---|---|---|---|
121062622 | 12106262 | 3 | 20160205 | 0 | ||
121062622 | 12106262 | 4 | 20160205 | 0 | ||
121062622 | 12106262 | 5 | 20160205 | 0 | ||
121062622 | 12106262 | 6 | 20160205 | 0 |