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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125944501 | 12594450 | 1 | I | 201512 | 20151204 | 20160726 | 20160726 | PER | US-UNITED THERAPEUTICS-UNT-2015-015474 | UNITED THERAPEUTICS | 43.64 | YR | M | Y | 80.73000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125944501 | 12594450 | 1 | PS | ORENITRAM | TREPROSTINIL | 1 | 0.75 MG, TID | U | U | 2100397 | 203496 | .75 | MG | TABLET | TID | ||||
| 125944501 | 12594450 | 2 | SS | TYVASO | TREPROSTINIL | 1 | U | U | 0 | INHALATION GAS | |||||||||
| 125944501 | 12594450 | 3 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 10 MG, QD | 1404527A | 0 | 10 | MG | TABLET | QD | |||||
| 125944501 | 12594450 | 4 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 10 MG, QD | 1408789A | 0 | 10 | MG | TABLET | QD | |||||
| 125944501 | 12594450 | 5 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 10 MG, QD | 1409095A | 0 | 10 | MG | TABLET | QD | |||||
| 125944501 | 12594450 | 6 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 10 MG, QD | SBFT | 0 | 10 | MG | TABLET | QD | |||||
| 125944501 | 12594450 | 7 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 10 MG,QD | SBFX | 0 | 10 | MG | TABLET | QD | |||||
| 125944501 | 12594450 | 8 | SS | REVATIO | SILDENAFIL CITRATE | 1 | Unknown | U | U | 0 | |||||||||
| 125944501 | 12594450 | 9 | SS | DILTIAZEM. | DILTIAZEM | 1 | Unknown | U | U | 0 | |||||||||
| 125944501 | 12594450 | 10 | C | VELETRI | EPOPROSTENOL | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125944501 | 12594450 | 1 | Pulmonary hypertension |
| 125944501 | 12594450 | 2 | Product used for unknown indication |
| 125944501 | 12594450 | 3 | Pulmonary hypertension |
| 125944501 | 12594450 | 4 | Heart disease congenital |
| 125944501 | 12594450 | 8 | Product used for unknown indication |
| 125944501 | 12594450 | 9 | Product used for unknown indication |
| 125944501 | 12594450 | 10 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125944501 | 12594450 | Dyspnoea exertional | |
| 125944501 | 12594450 | Headache | |
| 125944501 | 12594450 | Neck pain | |
| 125944501 | 12594450 | Pain | |
| 125944501 | 12594450 | Pain in extremity | |
| 125944501 | 12594450 | Pain in jaw |
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 |
|---|---|---|---|---|---|---|
| 125944501 | 12594450 | 1 | 20141226 | 0 | ||
| 125944501 | 12594450 | 3 | 20120817 | 0 |