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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127622811 | 12762281 | 1 | I | 20160601 | 0 | 20160915 | 20160915 | DIR | FDA-CTU | 67.00 | YR | M | N | 0.00000 | 20160819 | N | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127622811 | 12762281 | 1 | PS | DOEFETILIDE | DOFETILIDE | 1 | Oral | D | D | 0 | 0.5 | MG | BID | ||||||
127622811 | 12762281 | 2 | SS | TIKOSYN | DOFETILIDE | 1 | Oral | N | N | 0 | 0.5 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127622811 | 12762281 | 1 | Atrial fibrillation |
127622811 | 12762281 | 1 | Ventricular tachycardia |
127622811 | 12762281 | 2 | Atrial fibrillation |
127622811 | 12762281 | 2 | Ventricular tachycardia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127622811 | 12762281 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
127622811 | 12762281 | HP |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
127622811 | 12762281 | 1 | 20160723 | 0 | ||
127622811 | 12762281 | 2 | 20150425 | 20160722 | 0 |