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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124900552 | 12490055 | 2 | F | 20160523 | 20160804 | 20160622 | 20160811 | EXP | DE-ACTELION-A-US2016-138189 | ACTELION | 65.00 | YR | E | F | Y | 0.00000 | 20160811 | OT | DE | CO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124900552 | 12490055 | 1 | PS | VENTAVIS | ILOPROST | 1 | Respiratory (inhalation) | 1 DF, TID | 21779 | INHALATION VAPOUR, SOLUTION | TID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124900552 | 12490055 | 1 | Pulmonary hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124900552 | 12490055 | OT |
| 124900552 | 12490055 | DE |
| 124900552 | 12490055 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124900552 | 12490055 | Cardio-respiratory arrest | |
| 124900552 | 12490055 | Fatigue | |
| 124900552 | 12490055 | Lung infection | |
| 124900552 | 12490055 | Product use issue | |
| 124900552 | 12490055 | 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 |
|---|---|---|---|---|---|---|
| 124900552 | 12490055 | 1 | 20160523 | 20160609 | 0 |