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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125494961 | 12549496 | 1 | I | 20160623 | 20160712 | 20160712 | EXP | US-VALIDUS PHARMACEUTICALS LLC-US-2016VAL002205 | VALIDUS | 0.00 | Y | 0.00000 | 20160711 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125494961 | 12549496 | 1 | PS | LASIX | FUROSEMIDE | 1 | UNK | U | 16273 | ||||||||||
125494961 | 12549496 | 2 | SS | CARVEDILOL. | CARVEDILOL | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125494961 | 12549496 | 1 | Cardiac failure congestive |
125494961 | 12549496 | 2 | Cardiac failure congestive |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125494961 | 12549496 | OT |
125494961 | 12549496 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125494961 | 12549496 | Blood potassium increased | |
125494961 | 12549496 | Drug ineffective | |
125494961 | 12549496 | Dyspnoea | |
125494961 | 12549496 | Mobility decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |