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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125945051 | 12594505 | 1 | I | 201512 | 20151215 | 20160726 | 20160726 | PER | US-UNITED THERAPEUTICS-UNT-2015-015992 | UNITED THERAPEUTICS | 62.32 | YR | F | Y | 58.96000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125945051 | 12594505 | 1 | PS | ORENITRAM | TREPROSTINIL | 1 | Oral | 2 MG, TID | 2100398 | 203496 | 2 | MG | TABLET | TID | |||||
125945051 | 12594505 | 2 | SS | ORENITRAM | TREPROSTINIL | 1 | Oral | 2 MG, TID | 203496 | 2 | MG | TABLET | TID | ||||||
125945051 | 12594505 | 3 | SS | LETAIRIS | AMBRISENTAN | 1 | Oral | 10 MG, QD | 1404527A | 0 | 10 | MG | TABLET | QD | |||||
125945051 | 12594505 | 4 | SS | LETAIRIS | AMBRISENTAN | 1 | Oral | 10 MG, QD | 1404527A | 0 | 10 | MG | TABLET | QD | |||||
125945051 | 12594505 | 5 | SS | REVATIO | SILDENAFIL CITRATE | 1 | Oral | 20 MG, TID | 0 | 20 | MG | TID | |||||||
125945051 | 12594505 | 6 | C | LASIX | FUROSEMIDE | 1 | UNK | 0 | |||||||||||
125945051 | 12594505 | 7 | C | ALDACTONE | SPIRONOLACTONE | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125945051 | 12594505 | 1 | Pulmonary arterial hypertension |
125945051 | 12594505 | 2 | Pulmonary hypertension |
125945051 | 12594505 | 3 | Pulmonary arterial hypertension |
125945051 | 12594505 | 5 | Essential hypertension |
125945051 | 12594505 | 6 | Product used for unknown indication |
125945051 | 12594505 | 7 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125945051 | 12594505 | Abdominal discomfort | |
125945051 | 12594505 | Diarrhoea | |
125945051 | 12594505 | Dyspnoea exertional | |
125945051 | 12594505 | Flushing | |
125945051 | 12594505 | Headache |
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 |
---|---|---|---|---|---|---|
125945051 | 12594505 | 1 | 20150427 | 0 | ||
125945051 | 12594505 | 2 | 201505 | 0 | ||
125945051 | 12594505 | 3 | 20080601 | 0 | ||
125945051 | 12594505 | 4 | 20150226 | 0 | ||
125945051 | 12594505 | 5 | 200803 | 0 | ||
125945051 | 12594505 | 6 | 2007 | 0 |