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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125268195 | 12526819 | 5 | F | 201606 | 20160719 | 20160705 | 20160725 | EXP | US-UNITED THERAPEUTICS-UNT-2016-010572 | UNITED THERAPEUTICS | 66.78 | YR | F | Y | 61.22000 | KG | 20160725 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125268195 | 12526819 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Intravenous drip | 0.046 ?G/KG, CONTINUING | U | U | 2100910 | 21272 | .046 | UG/KG | INJECTION | ||||
| 125268195 | 12526819 | 2 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 5 MG, QD | U | U | 1412805A | 0 | 5 | MG | QD | ||||
| 125268195 | 12526819 | 3 | C | ADCIRCA | TADALAFIL | 1 | UNK | 0 | |||||||||||
| 125268195 | 12526819 | 4 | C | COUMADIN | WARFARIN SODIUM | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125268195 | 12526819 | 1 | Pulmonary arterial hypertension |
| 125268195 | 12526819 | 2 | Product used for unknown indication |
| 125268195 | 12526819 | 3 | Product used for unknown indication |
| 125268195 | 12526819 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125268195 | 12526819 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125268195 | 12526819 | Altered state of consciousness | |
| 125268195 | 12526819 | Asthenia | |
| 125268195 | 12526819 | Cough | |
| 125268195 | 12526819 | Device use error | |
| 125268195 | 12526819 | Diarrhoea | |
| 125268195 | 12526819 | Flushing | |
| 125268195 | 12526819 | Hypoxia | |
| 125268195 | 12526819 | Malaise | |
| 125268195 | 12526819 | Pallor | |
| 125268195 | 12526819 | Presyncope | |
| 125268195 | 12526819 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 125268195 | 12526819 | 1 | 20150708 | 0 |