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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7583249 | 8016711 | I | 7583249-9 | 20110501 | 20110623 | 20110630 | EXP | US-ACTELION-A-US2011-50851 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7583249 | 1016903698 | C | REVATIO | 1 | |||||||
7583249 | 1016903697 | PS | TRACLEER | 1 | ORAL | UNK | EP076P0101 | 021290 | |||
7583249 | 1016903699 | C | COUMADIN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7583249 | 1016903697 | PULMONARY ARTERIAL HYPERTENSION |
Outcome of event
Event ID | OUTC COD |
---|---|
7583249 | DE |
Reactions reported
Event ID | PT |
---|---|
7583249 | DEATH |
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 |
---|---|---|---|---|---|
7583249 | 1016903697 | 20050825 |