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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4390003 | 4145186 | F | 1 | 4390003-8 | 20040420 | 20040618 | 20040630 | EXP | A-CH2004-06142 | ACTELION PHARMACEUTICALS US, INC | 34 | YR | F | N | 55 | KG | 20040629 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4390003 | 1004988344 | PS | TRACLEER | 1 | ORAL | 62.5 MG, BID, ORAL | Y | D | 21290 | ||
| 4390003 | 1005006466 | C | ILOPROST (ILOPROST) | 2 | |||||||
| 4390003 | 1005006467 | C | SILENAFIL | 2 | |||||||
| 4390003 | 1005006469 | C | PREDNISOLONE | 1 | |||||||
| 4390003 | 1005006470 | C | WARFARIN SODIUM | 1 | |||||||
| 4390003 | 1005006471 | C | FUROSEMIDE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4390003 | 1004988344 | PULMONARY HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4390003 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4390003 | ABDOMINAL PAIN |
| 4390003 | ABDOMINAL PAIN UPPER |
| 4390003 | ARTHRALGIA |
| 4390003 | HEADACHE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4390003 | FGN |
| 4390003 | HP |
| 4390003 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4390003 | 1004988344 | 20040414 | 20040503 |