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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 92006661 | 9200666 | 1 | I | 2010 | 20130228 | 20130331 | 20130331 | PER | US-ASTRAZENECA-2013SE14116 | ASTRAZENECA | 81.00 | YR | F | Y | 56.70000 | KG | 20130331 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 92006661 | 9200666 | 1 | PS | SYMBICORT PMDI | 1 | INHALATION | 2 PUFFS TWO TIMES A DAY | D | 21929 | BID | |||||||||
| 92006661 | 9200666 | 2 | SS | CRESTOR | 1 | ORAL | 25570 | MG | D | 0 | 10 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 92006661 | 9200666 | 1 | Asthma |
| 92006661 | 9200666 | 2 | Blood cholesterol increased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 92006661 | 9200666 | Dizziness | |
| 92006661 | 9200666 | Hypertension | |
| 92006661 | 9200666 | Myalgia | |
| 92006661 | 9200666 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 92006661 | 9200666 | 2 | 2003 | 0 |