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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124723223 | 12472322 | 3 | F | 20160805 | 20160616 | 20160815 | PER | US-ACTELION-A-US2014-101342 | ACTELION | 58.00 | YR | A | F | Y | 0.00000 | 20160815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124723223 | 12472322 | 1 | PS | VELETRI | EPOPROSTENOL | 1 | Intravenous (not otherwise specified) | 8 NG/KG, PER MIN | MM034M0101/MM035M0301/MM038M0301 | 22260 | INJECTION | /min | |||||||
| 124723223 | 12472322 | 2 | SS | VELETRI | EPOPROSTENOL | 1 | Intravenous (not otherwise specified) | 10 NG/KG, PER MIN | MM035M0301, MM083M0101 | 22260 | INJECTION | /min | |||||||
| 124723223 | 12472322 | 3 | SS | VELETRI | EPOPROSTENOL | 1 | Intravenous (not otherwise specified) | 20 NG/KG, PER MIN | MM044M0101 | 22260 | INJECTION | /min | |||||||
| 124723223 | 12472322 | 4 | SS | VELETRI | EPOPROSTENOL | 1 | Intravenous (not otherwise specified) | 26 NG/KG PER MIN | 22260 | INJECTION | /min | ||||||||
| 124723223 | 12472322 | 5 | SS | ADCIRCA | TADALAFIL | 1 | Unknown | U | U | 0 | |||||||||
| 124723223 | 12472322 | 6 | C | RIOCIGUAT | RIOCIGUAT | 1 | 1 MG, TID | U | 0 | 1 | MG | TID | |||||||
| 124723223 | 12472322 | 7 | C | LETAIRIS | AMBRISENTAN | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124723223 | 12472322 | 1 | Pulmonary hypertension |
| 124723223 | 12472322 | 5 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124723223 | 12472322 | Agitation | |
| 124723223 | 12472322 | Anxiety | |
| 124723223 | 12472322 | Diarrhoea | |
| 124723223 | 12472322 | Dyspnoea | |
| 124723223 | 12472322 | Insomnia | |
| 124723223 | 12472322 | Limb discomfort | |
| 124723223 | 12472322 | Pain in jaw | |
| 124723223 | 12472322 | Rash generalised | |
| 124723223 | 12472322 | Restless legs syndrome | |
| 124723223 | 12472322 | Restlessness |
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 |
|---|---|---|---|---|---|---|
| 124723223 | 12472322 | 1 | 20140605 | 0 | ||
| 124723223 | 12472322 | 2 | 20140625 | 0 | ||
| 124723223 | 12472322 | 6 | 20140326 | 0 |