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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6772968 | 7428095 | I | 6772968-X | 20100521 | 20100527 | 20100614 | EXP | A-NJ2010-37010 | ACTELION PHARMACEUTICALS US, INC. | 40 | YR | F | N | 20100608 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6772968 | 1013880076 | PS | TRACLEER | 1 | ORAL | 125 MG, BID, ORAL, 62.5 MG, BID, ORAL | D | D | 21290 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6772968 | 1013880076 | PULMONARY ARTERIAL HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6772968 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6772968 | DEPRESSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6772968 | DT |
| 6772968 | HP |
| 6772968 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6772968 | 1013880076 | 20020801 |