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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125943841 | 12594384 | 1 | I | 20160103 | 20160105 | 20160726 | 20160726 | EXP | US-UNITED THERAPEUTICS-UNT-2016-000197 | UNITED THERAPEUTICS | 20.57 | YR | F | Y | 63.40000 | KG | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125943841 | 12594384 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.090 ?G/KG, CONTINUING | 2100666 | 21272 | .09 | UG/KG | INJECTION | ||||||
| 125943841 | 12594384 | 2 | SS | LETAIRIS | AMBRISENTAN | 1 | Oral | 10 MG, QD | SBFW | 0 | 10 | MG | TABLET | QD | |||||
| 125943841 | 12594384 | 3 | SS | LETAIRIS | AMBRISENTAN | 1 | Oral | UNK | 1503901A | 0 | TABLET | ||||||||
| 125943841 | 12594384 | 4 | SS | ADCIRCA | TADALAFIL | 1 | Unknown | UNK | Y | 0 | |||||||||
| 125943841 | 12594384 | 5 | C | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 125943841 | 12594384 | 6 | C | PEPCID /00305201/ | ALUMINUM HYDROXIDEMAGNESIUM CARBONATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125943841 | 12594384 | 1 | Pulmonary arterial hypertension |
| 125943841 | 12594384 | 2 | Pulmonary arterial hypertension |
| 125943841 | 12594384 | 4 | Product used for unknown indication |
| 125943841 | 12594384 | 5 | Product used for unknown indication |
| 125943841 | 12594384 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125943841 | 12594384 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125943841 | 12594384 | Chest pain | |
| 125943841 | 12594384 | Dizziness | |
| 125943841 | 12594384 | Dyspnoea | |
| 125943841 | 12594384 | Haemoptysis | |
| 125943841 | 12594384 | Pulmonary arterial hypertension |
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 |
|---|---|---|---|---|---|---|
| 125943841 | 12594384 | 1 | 20100824 | 0 | ||
| 125943841 | 12594384 | 2 | 20130614 | 0 | ||
| 125943841 | 12594384 | 4 | 201601 | 0 |