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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125800532 | 12580053 | 2 | F | 201606 | 20160713 | 20160721 | 20160721 | EXP | US-SA-2016SA129806 | AVENTIS | 78.00 | YR | E | M | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125800532 | 12580053 | 1 | PS | MULTAQ | DRONEDARONE | 1 | Unknown | U | 5T05433 | 22425 | 400 | MG | BID | ||||||
| 125800532 | 12580053 | 2 | SS | MULTAQ | DRONEDARONE | 1 | Unknown | U | UNKNOWN | 22425 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125800532 | 12580053 | 1 | Atrial fibrillation |
| 125800532 | 12580053 | 2 | Atrial fibrillation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125800532 | 12580053 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125800532 | 12580053 | Cardiac valve disease | |
| 125800532 | 12580053 | Drug ineffective | |
| 125800532 | 12580053 | Heart rate irregular | |
| 125800532 | 12580053 | 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 |
|---|---|---|---|---|---|---|
| 125800532 | 12580053 | 1 | 201302 | 20160712 | 0 |