Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7583250 | 8016712 | I | 7583250-5 | 20110101 | 20110621 | 20110630 | EXP | US-ACTELION-A-US2011-50716 | ACTELION | YR | Y | 20110630 | PH | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7583250 | 1016903700 | PS | TRACLEER | 1 | ORAL | UNK | EP078P0102 | 021290 | |||
| 7583250 | 1016903701 | C | CALCIUM CHANNEL BLOCKERS | 2 | |||||||
| 7583250 | 1016903702 | C | COUMADIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7583250 | 1016903700 | PULMONARY ARTERIAL HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7583250 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7583250 | PRESYNCOPE |
| 7583250 | BLOOD PRESSURE INCREASED |
| 7583250 | HEART RATE DECREASED |
| 7583250 | FALL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7583250 | 1016903700 | 20040406 |