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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117725803 | 11772580 | 3 | F | 201511 | 20151230 | 20151124 | 20160726 | EXP | US-UNITED THERAPEUTICS-UNT-2015-014712 | UNITED THERAPEUTICS | 54.70 | YR | F | Y | 46.26000 | KG | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117725803 | 11772580 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.037 ?G/KG, CONTINUING | U | U | 2100431 | 21272 | .037 | UG/KG | INJECTION | ||||
| 117725803 | 11772580 | 2 | SS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.022 ?G/KG, CONTINUING | U | U | 2100498 | 21272 | .022 | UG/KG | INJECTION | ||||
| 117725803 | 11772580 | 3 | SS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.021 ?G/KG, CONTINUING | U | U | 2100579 | 21272 | .021 | UG/KG | INJECTION | ||||
| 117725803 | 11772580 | 4 | C | ADCIRCA | TADALAFIL | 1 | 0 | ||||||||||||
| 117725803 | 11772580 | 5 | C | COUMADIN | WARFARIN SODIUM | 1 | 0 | ||||||||||||
| 117725803 | 11772580 | 6 | C | NORVASC | AMLODIPINE BESYLATE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117725803 | 11772580 | 1 | Pulmonary arterial hypertension |
| 117725803 | 11772580 | 4 | Product used for unknown indication |
| 117725803 | 11772580 | 5 | Product used for unknown indication |
| 117725803 | 11772580 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117725803 | 11772580 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117725803 | 11772580 | Chest pain | |
| 117725803 | 11772580 | Dyspnoea | |
| 117725803 | 11772580 | Malaise | |
| 117725803 | 11772580 | Pulmonary hypertension | |
| 117725803 | 11772580 | Suture rupture | |
| 117725803 | 11772580 | Vomiting | |
| 117725803 | 11772580 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 117725803 | 11772580 | 1 | 20141217 | 0 |