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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125442371 | 12544237 | 1 | I | 20160704 | 20160711 | 20160711 | EXP | SE-ORION CORPORATION ORION PHARMA-SPIR2016-0005 | ORION | 94.00 | YR | F | Y | 0.00000 | 20160711 | OT | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125442371 | 12544237 | 1 | PS | SPIRONOLACTONE (TRADE NAME UNKNOWN) | SPIRONOLACTONE | 1 | Unknown | STRENGTH: 25 MG | U | 0 | TABLET | ||||||||
| 125442371 | 12544237 | 2 | SS | FURIX | FUROSEMIDE | 1 | Unknown | STRENGTH: 40 MG | U | 0 | TABLET | ||||||||
| 125442371 | 12544237 | 3 | SS | CARVEDILOL. | CARVEDILOL | 1 | Unknown | STRENGTH: 12.5 MG | U | 0 | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125442371 | 12544237 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125442371 | 12544237 | Dizziness | |
| 125442371 | 12544237 | Syncope |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |