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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126580351 | 12658035 | 1 | I | 20160726 | 20160811 | 20160817 | 20160817 | EXP | FR-ASTRAZENECA-2016SE87335 | ASTRAZENECA | 95.00 | YR | F | Y | 0.00000 | 20160817 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126580351 | 12658035 | 1 | PS | ATACAND | CANDESARTAN CILEXETIL | 1 | Oral | 8.0MG ONCE/SINGLE ADMINISTRATION | 8 | MG | 20838 | 8 | MG | TABLET | |||||
| 126580351 | 12658035 | 2 | SS | SOTALOL. | SOTALOL | 1 | Oral | 80.0MG ONCE/SINGLE ADMINISTRATION | 80 | MG | 0 | 80 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126580351 | 12658035 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126580351 | 12658035 | Bradycardia | |
| 126580351 | 12658035 | Drug administration error | |
| 126580351 | 12658035 | Hypotension |
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 |
|---|---|---|---|---|---|---|
| 126580351 | 12658035 | 1 | 20160726 | 20160726 | 0 | |
| 126580351 | 12658035 | 2 | 20160726 | 20160726 | 0 |