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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125792712 | 12579271 | 2 | F | 201607 | 20160729 | 20160721 | 20160808 | EXP | US-UNITED THERAPEUTICS-UNT-2016-011367 | UNITED THERAPEUTICS | 29.69 | YR | F | Y | 68.27000 | KG | 20160808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125792712 | 12579271 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.085 ?G/KG, CONTINUING | 2100701 | 21272 | .085 | UG/KG | INJECTION | ||||||
| 125792712 | 12579271 | 2 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 0 | ||||||||||||
| 125792712 | 12579271 | 3 | C | COUMADIN | WARFARIN SODIUM | 1 | 0 | ||||||||||||
| 125792712 | 12579271 | 4 | C | ADCIRCA | TADALAFIL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125792712 | 12579271 | 1 | Pulmonary arterial hypertension |
| 125792712 | 12579271 | 2 | Product used for unknown indication |
| 125792712 | 12579271 | 3 | Product used for unknown indication |
| 125792712 | 12579271 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125792712 | 12579271 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125792712 | 12579271 | Device issue | |
| 125792712 | 12579271 | Dizziness | |
| 125792712 | 12579271 | Fatigue | |
| 125792712 | 12579271 | Headache | |
| 125792712 | 12579271 | Injection site discharge | |
| 125792712 | 12579271 | Nausea | |
| 125792712 | 12579271 | Syncope | |
| 125792712 | 12579271 | 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 |
|---|---|---|---|---|---|---|
| 125792712 | 12579271 | 1 | 20140307 | 0 |