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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125910562 | 12591056 | 2 | F | 201512 | 20160217 | 20160726 | 20160726 | PER | US-UNITED THERAPEUTICS-UNT-2015-015705 | UNITED THERAPEUTICS | 62.77 | YR | M | Y | 89.80000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125910562 | 12591056 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.070 ?G/KG/MIN, CONTINUING | U | U | 2100665 | 21272 | .07 | UG/KG | INJECTION | ||||
125910562 | 12591056 | 2 | SS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.067 ?G/KG/MIN, UNK | U | U | 2100666 | 21272 | .067 | UG/KG | INJECTION | ||||
125910562 | 12591056 | 3 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | 5 MG, QD | SBFP | 0 | 5 | MG | TABLET | QD | |||||
125910562 | 12591056 | 4 | SS | ADCIRCA | TADALAFIL | 1 | Unknown | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125910562 | 12591056 | 1 | Pulmonary arterial hypertension |
125910562 | 12591056 | 3 | Product used for unknown indication |
125910562 | 12591056 | 4 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125910562 | 12591056 | Chest pain | |
125910562 | 12591056 | Device occlusion | |
125910562 | 12591056 | Drug dose omission | |
125910562 | 12591056 | Infusion site erythema | |
125910562 | 12591056 | Infusion site pain | |
125910562 | 12591056 | Pain in extremity |
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 |
---|---|---|---|---|---|---|
125910562 | 12591056 | 1 | 20150529 | 0 | ||
125910562 | 12591056 | 3 | 20130624 | 0 |