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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127006511 | 12700651 | 1 | I | 20151202 | 20151207 | 20160830 | 20160830 | PER | US-SA-2015SA209231 | AVENTIS | 68.00 | YR | E | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127006511 | 12700651 | 1 | PS | MULTAQ | DRONEDARONE | 1 | Unknown | GH054 | 22425 | 400 | MG | BID | |||||||
| 127006511 | 12700651 | 2 | I | ELIQUIS | APIXABAN | 1 | Unknown | N | UNK | 0 | |||||||||
| 127006511 | 12700651 | 3 | C | SOTALOL. | SOTALOL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127006511 | 12700651 | 1 | Surgery |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127006511 | 12700651 | Diarrhoea | |
| 127006511 | 12700651 | Drug interaction | |
| 127006511 | 12700651 | Haematuria | |
| 127006511 | 12700651 | Muscle spasms | |
| 127006511 | 12700651 | Paraesthesia | |
| 127006511 | 12700651 | Visual acuity reduced |
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 |
|---|---|---|---|---|---|---|
| 127006511 | 12700651 | 1 | 20151126 | 0 |