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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125828432 | 12582843 | 2 | F | 20160715 | 20160822 | 20160722 | 20160829 | EXP | US-UNITED THERAPEUTICS-UNT-2016-011572 | UNITED THERAPEUTICS | 40.71 | YR | F | Y | 160.54000 | KG | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125828432 | 12582843 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Intravenous drip | 0.026 ?G/KG, CONTINUING | U | U | 2100956 | 21272 | .026 | UG/KG | INJECTION | ||||
125828432 | 12582843 | 2 | C | LETAIRIS | AMBRISENTAN | 1 | 0 | ||||||||||||
125828432 | 12582843 | 3 | C | COUMADIN | WARFARIN SODIUM | 1 | 0 | ||||||||||||
125828432 | 12582843 | 4 | C | REVATIO | SILDENAFIL CITRATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125828432 | 12582843 | 1 | Pulmonary arterial hypertension |
125828432 | 12582843 | 2 | Product used for unknown indication |
125828432 | 12582843 | 3 | Product used for unknown indication |
125828432 | 12582843 | 4 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125828432 | 12582843 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125828432 | 12582843 | Blood potassium decreased | |
125828432 | 12582843 | Malaise |
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 |
---|---|---|---|---|---|---|
125828432 | 12582843 | 1 | 20150805 | 0 |