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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127905081 | 12790508 | 1 | I | 20160318 | 20160920 | 20160929 | 20160929 | EXP | DE-ACTELION-A-US2016-143040 | ACTELION | 26.00 | YR | A | F | Y | 0.00000 | 20160929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127905081 | 12790508 | 1 | PS | VENTAVIS | ILOPROST | 1 | Respiratory (inhalation) | 2.5 MCG, Q4HRS | U | U | 21779 | 2.5 | UG | INHALATION VAPOUR, SOLUTION | Q4H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127905081 | 12790508 | 1 | Pulmonary arterial hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127905081 | 12790508 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127905081 | 12790508 | Asphyxia | |
| 127905081 | 12790508 | Drug intolerance | |
| 127905081 | 12790508 | Dyspnoea | |
| 127905081 | 12790508 | Erythema | |
| 127905081 | 12790508 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 127905081 | 12790508 | 1 | 20160318 | 0 |