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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125914702 | 12591470 | 2 | F | 201512 | 20160128 | 20160726 | 20160726 | PER | US-UNITED THERAPEUTICS-UNT-2016-000273 | UNITED THERAPEUTICS | 30.95 | YR | F | Y | 70.30000 | KG | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125914702 | 12591470 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.0892 ?G/KG, CONTINUING | U | U | 2100665 | 21272 | .089 | UG/KG | INJECTION | ||||
| 125914702 | 12591470 | 2 | SS | LETAIRIS | AMBRISENTAN | 1 | Oral | 10 MG, QD | SBFW | 0 | 10 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125914702 | 12591470 | 1 | Pulmonary arterial hypertension |
| 125914702 | 12591470 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125914702 | 12591470 | Hypotension | |
| 125914702 | 12591470 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 125914702 | 12591470 | 1 | 20140910 | 0 | ||
| 125914702 | 12591470 | 2 | 20141022 | 0 |