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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125948321 | 12594832 | 1 | I | 201601 | 20160303 | 20160726 | 20160726 | PER | US-UNITED THERAPEUTICS-UNT-2016-003674 | UNITED THERAPEUTICS | 72.93 | YR | F | Y | 87.75000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125948321 | 12594832 | 1 | PS | TYVASO | TREPROSTINIL | 1 | 18-54 MICROGRAMS, QID | U | U | 2100715 | 22387 | INHALATION GAS | QID | ||||||
| 125948321 | 12594832 | 2 | SS | TYVASO | TREPROSTINIL | 1 | U | U | 22387 | INHALATION GAS | |||||||||
| 125948321 | 12594832 | 3 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 10 MG, QD | 1500225A | 0 | 10 | MG | TABLET | QD | |||||
| 125948321 | 12594832 | 4 | SS | LETAIRIS | AMBRISENTAN | 1 | UNK | 1500227A | 0 | TABLET | |||||||||
| 125948321 | 12594832 | 5 | SS | LETAIRIS | AMBRISENTAN | 1 | UNK | 1503901A | 0 | TABLET | |||||||||
| 125948321 | 12594832 | 6 | SS | REVATIO | SILDENAFIL CITRATE | 1 | Unknown | U | U | 0 | |||||||||
| 125948321 | 12594832 | 7 | C | WARFARIN | WARFARIN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125948321 | 12594832 | 1 | Pulmonary hypertension |
| 125948321 | 12594832 | 2 | Pulmonary arterial hypertension |
| 125948321 | 12594832 | 3 | Product used for unknown indication |
| 125948321 | 12594832 | 6 | Product used for unknown indication |
| 125948321 | 12594832 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125948321 | 12594832 | Back pain | |
| 125948321 | 12594832 | Diarrhoea | |
| 125948321 | 12594832 | Drug titration error | |
| 125948321 | 12594832 | Erythema | |
| 125948321 | 12594832 | Flushing | |
| 125948321 | 12594832 | Headache | |
| 125948321 | 12594832 | Influenza like illness | |
| 125948321 | 12594832 | Malaise | |
| 125948321 | 12594832 | Muscle tightness | |
| 125948321 | 12594832 | Myalgia | |
| 125948321 | 12594832 | Nasal congestion | |
| 125948321 | 12594832 | Nausea | |
| 125948321 | 12594832 | Pain | |
| 125948321 | 12594832 | Pain in extremity | |
| 125948321 | 12594832 | Seasonal allergy |
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 |
|---|---|---|---|---|---|---|
| 125948321 | 12594832 | 1 | 20130918 | 201601 | 0 | |
| 125948321 | 12594832 | 3 | 20150202 | 0 |