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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126462761 | 12646276 | 1 | I | 2014 | 20160804 | 20160812 | 20160812 | EXP | US-ASTRAZENECA-2016SE85839 | ASTRAZENECA | 0.00 | M | Y | 0.00000 | 20160812 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126462761 | 12646276 | 1 | PS | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | TWO PUFFS TWICE A DAY | Y | UNKNOWN | 21929 | ||||||||
| 126462761 | 12646276 | 2 | C | VICTOZA | LIRAGLUTIDE | 1 | INJECTABLE PEN | 0 | |||||||||||
| 126462761 | 12646276 | 3 | C | BRIO | 2 | INJECTABLE PEN | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126462761 | 12646276 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126462761 | 12646276 | Accident | |
| 126462761 | 12646276 | Coma | |
| 126462761 | 12646276 | Drug ineffective | |
| 126462761 | 12646276 | Intentional product misuse | |
| 126462761 | 12646276 | Pulmonary embolism | |
| 126462761 | 12646276 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |