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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125911412 | 12591141 | 2 | F | 201603 | 20160317 | 20160726 | 20160727 | PER | US-UNITED THERAPEUTICS-UNT-2016-004530 | UNITED THERAPEUTICS | 48.50 | YR | F | Y | 75.28000 | KG | 20160727 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125911412 | 12591141 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Intravenous drip | 0.028 ?G/KG, CONTINUING | U | U | 926618 | 21272 | .028 | UG/KG | INJECTION | ||||
125911412 | 12591141 | 2 | SS | REMODULIN | TREPROSTINIL | 1 | Intravenous drip | 0.030 ?G/KG, CONTINUING | U | U | 21272 | .03 | UG/KG | INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125911412 | 12591141 | 1 | Pulmonary arterial hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125911412 | 12591141 | Diarrhoea | |
125911412 | 12591141 | Dizziness postural | |
125911412 | 12591141 | 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 |
---|---|---|---|---|---|---|
125911412 | 12591141 | 1 | 20151218 | 0 | ||
125911412 | 12591141 | 2 | 20160312 | 0 |