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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126537601 | 12653760 | 1 | I | 20160724 | 20160801 | 20160816 | 20160816 | PER | US-ASTRAZENECA-2016SE83376 | ASTRAZENECA | 27600.00 | DY | M | Y | 70.30000 | KG | 20160816 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126537601 | 12653760 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80/4.5, ONE PUFF TWICE DAILY | 21929 | ||||||||||
126537601 | 12653760 | 2 | SS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | 80/4.5, 2 PUFFS TWICE DAILY | 21929 | ||||||||||
126537601 | 12653760 | 3 | C | COERIG | 2 | 0 | |||||||||||||
126537601 | 12653760 | 4 | C | VYTORIN | EZETIMIBESIMVASTATIN | 1 | 0 | QD | |||||||||||
126537601 | 12653760 | 5 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | 0 | QD | |||||||||||
126537601 | 12653760 | 6 | C | DIAVAN | ASCORBIC ACID/ CHROMIUM/ SELENIUM/VANADYL SULFATE | 1 | 0 | QD | |||||||||||
126537601 | 12653760 | 7 | C | MONOLUKAST | 2 | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126537601 | 12653760 | 1 | Asthma |
126537601 | 12653760 | 2 | Asthma |
126537601 | 12653760 | 3 | Cardiac disorder |
126537601 | 12653760 | 4 | Blood cholesterol abnormal |
126537601 | 12653760 | 5 | Cardiac disorder |
126537601 | 12653760 | 6 | Cardiac disorder |
126537601 | 12653760 | 7 | Asthma |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126537601 | 12653760 | Intentional product misuse | |
126537601 | 12653760 | Upper-airway cough syndrome | |
126537601 | 12653760 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |