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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125797662 | 12579766 | 2 | F | 20160712 | 20160810 | 20160721 | 20160819 | EXP | US-UNITED THERAPEUTICS-UNT-2016-011289 | UNITED THERAPEUTICS | 65.98 | YR | F | Y | 86.17000 | KG | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125797662 | 12579766 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Intravenous drip | 0.031 ?G/KG, CONTINUING | 2100955 | 21272 | .031 | UG/KG | INJECTION | ||||||
| 125797662 | 12579766 | 2 | C | DILTIAZEM. | DILTIAZEM | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125797662 | 12579766 | 1 | Pulmonary arterial hypertension |
| 125797662 | 12579766 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125797662 | 12579766 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125797662 | 12579766 | Dyspnoea | |
| 125797662 | 12579766 | Fluid retention | |
| 125797662 | 12579766 | Nausea | |
| 125797662 | 12579766 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 125797662 | 12579766 | 1 | 20160328 | 0 |