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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125258851 | 12525885 | 1 | I | 20160614 | 20160620 | 20160705 | 20160705 | PER | US-ASTRAZENECA-2016SE72177 | ASTRAZENECA | 0.00 | A | M | Y | 99.80000 | KG | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125258851 | 12525885 | 1 | PS | RHINOCORT ALLERGY | BUDESONIDE | 1 | Nasal | 4 | DF | Y | U | VACK | 20746 | 2 | DF | NASAL SPRAY | QD | ||
| 125258851 | 12525885 | 2 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | Unknown | 0 | 25 | MG | BID | ||||||||
| 125258851 | 12525885 | 3 | C | VYTORIN | EZETIMIBESIMVASTATIN | 1 | Unknown | 0 | 1040 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125258851 | 12525885 | 1 | Product used for unknown indication |
| 125258851 | 12525885 | 2 | Hypertension |
| 125258851 | 12525885 | 3 | Blood cholesterol increased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125258851 | 12525885 | Headache |
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 |
|---|---|---|---|---|---|---|
| 125258851 | 12525885 | 1 | 20160613 | 20160617 | 0 |