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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125225803 | 12522580 | 3 | F | 201606 | 20160822 | 20160701 | 20160901 | EXP | US-ACTELION-A-NJ2016-134552 | ACTELION | 69.00 | YR | E | F | Y | 0.00000 | 20160901 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125225803 | 12522580 | 1 | PS | TRACLEER | BOSENTAN | 1 | Oral | 125 MG, BID | OP021P0101,OP023P0101,OP026P0101 | 21290 | 125 | MG | TABLET | BID | |||||
125225803 | 12522580 | 2 | C | TYVASO | TREPROSTINIL | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125225803 | 12522580 | 1 | Pulmonary hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125225803 | 12522580 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125225803 | 12522580 | Arthritis | |
125225803 | 12522580 | Infection | |
125225803 | 12522580 | Joint swelling | |
125225803 | 12522580 | Oedema peripheral | |
125225803 | 12522580 | Pain in extremity | |
125225803 | 12522580 | Pyrexia |
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 |
---|---|---|---|---|---|---|
125225803 | 12522580 | 1 | 20150911 | 0 |