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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127006501 | 12700650 | 1 | I | 20151031 | 20151204 | 20160830 | 20160830 | PER | US-SA-2015SA208890 | AVENTIS | 69.00 | YR | E | F | Y | 0.00000 | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127006501 | 12700650 | 1 | PS | MULTAQ | DRONEDARONE | 1 | Unknown | Y | 5T01332 | 22425 | 400 | MG | BID | ||||||
| 127006501 | 12700650 | 2 | C | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | 0 | ||||||||||||
| 127006501 | 12700650 | 3 | C | GLIPIZIDE. | GLIPIZIDE | 1 | 0 | ||||||||||||
| 127006501 | 12700650 | 4 | C | CARVEDILOL. | CARVEDILOL | 1 | 0 | ||||||||||||
| 127006501 | 12700650 | 5 | C | PRAVASTATIN SODIUM. | PRAVASTATIN SODIUM | 1 | 0 | ||||||||||||
| 127006501 | 12700650 | 6 | C | LOSARTAN. | LOSARTAN | 1 | 0 | ||||||||||||
| 127006501 | 12700650 | 7 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127006501 | 12700650 | 1 | Atrial fibrillation |
| 127006501 | 12700650 | 2 | Anticoagulant therapy |
| 127006501 | 12700650 | 3 | Blood glucose increased |
| 127006501 | 12700650 | 5 | Hypertension |
| 127006501 | 12700650 | 6 | Blood pressure measurement |
| 127006501 | 12700650 | 7 | Cardiac disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127006501 | 12700650 | Abdominal discomfort | |
| 127006501 | 12700650 | Asthenia | |
| 127006501 | 12700650 | Dizziness | |
| 127006501 | 12700650 | Fatigue | |
| 127006501 | 12700650 | Heart rate increased | |
| 127006501 | 12700650 | Malaise | |
| 127006501 | 12700650 | Mobility decreased | |
| 127006501 | 12700650 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 127006501 | 12700650 | 1 | 20151003 | 20151103 | 0 | |
| 127006501 | 12700650 | 2 | 2000 | 0 | ||
| 127006501 | 12700650 | 3 | 2015 | 0 | ||
| 127006501 | 12700650 | 5 | 2010 | 0 | ||
| 127006501 | 12700650 | 6 | 2010 | 0 | ||
| 127006501 | 12700650 | 7 | 2015 | 0 |