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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6140955 | 6965800 | I | 6140955-0 | 20090313 | 20090317 | 20090331 | EXP | A-CH2009-24386 | ACTELION PHARMACEUTICALS US, INC. | 33 | YR | F | N | 56 | KG | 20090330 | CN | GREECE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6140955 | 1011367858 | PS | TRACLEER | 1 | ORAL | 125 MG, BID, ORAL | D | D | 21290 | ||
| 6140955 | 1011408706 | C | THYROHORMONE (LEVOTHYROXINE SODIUM) | 2 | |||||||
| 6140955 | 1011408781 | C | SALOSPIR (ACETYLSALICYLIC ACID) | 2 | |||||||
| 6140955 | 1011408783 | C | ONEALFA (ALFACALCIDOL) | 2 | |||||||
| 6140955 | 1011408784 | C | DEFEROXAMINE (DEFEROXAMINE) | 2 | |||||||
| 6140955 | 1011408785 | C | DEFERIPRONE (DEFERIPRONE) | 2 | |||||||
| 6140955 | 1011408787 | C | CARNITINE (CARNITINE) | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6140955 | 1011367858 | PULMONARY ARTERIAL HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6140955 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6140955 | DRUG EXPOSURE DURING PREGNANCY |
| 6140955 | PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6140955 | FGN |
| 6140955 | HP |
| 6140955 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6140955 | 1011367858 | 20080729 | 20090313 |