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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 115541952 | 11554195 | 2 | F | 20160818 | 20150925 | 20160825 | PER | US-ACTELION PHARMACEUTICALS US, INC.-A-US2014-107153 | ACTELION | 72.00 | YR | E | F | Y | 0.00000 | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 115541952 | 11554195 | 1 | PS | TRACLEER | BOSENTAN | 1 | Oral | 62.5 MG, UNK | 0P010A0102,IP050P0101,NP011A0101 | 21290 | 62.5 | MG | TABLET | ||||||
| 115541952 | 11554195 | 2 | SS | SILDENAFIL. | SILDENAFIL | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 115541952 | 11554195 | 1 | Pulmonary arterial hypertension |
| 115541952 | 11554195 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 115541952 | 11554195 | Condition aggravated | |
| 115541952 | 11554195 | Seasonal allergy | |
| 115541952 | 11554195 | Sinus congestion | |
| 115541952 | 11554195 | Sinus disorder |
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 |
|---|---|---|---|---|---|---|
| 115541952 | 11554195 | 1 | 20140716 | 0 |