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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125911532 | 12591153 | 2 | F | 201603 | 20160418 | 20160726 | 20160727 | PER | US-UNITED THERAPEUTICS-UNT-2016-004377 | UNITED THERAPEUTICS | 44.28 | YR | F | Y | 70.75000 | KG | 20160727 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125911532 | 12591153 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.031 ?G/KG, CONTINUING | 2100664 | 21272 | .031 | UG/KG | INJECTION | ||||||
| 125911532 | 12591153 | 2 | C | TRACLEER | BOSENTAN | 1 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125911532 | 12591153 | Cardiac failure congestive | |
| 125911532 | 12591153 | Drug titration error | |
| 125911532 | 12591153 | Oedema peripheral | |
| 125911532 | 12591153 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 125911532 | 12591153 | 1 | 20150302 | 0 |