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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7583248 | 7999757 | F | 7583248-7 | 20110601 | 20110623 | 20110630 | EXP | US-ACTELION-A-US2011-50299 | ACTELION | YR | Y | 20110630 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7583248 | 1016903696 | PS | TRACLEER | 1 | ORAL | UNK | EP079P0201 | 021290 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7583248 | 1016903696 | PULMONARY ARTERIAL HYPERTENSION |
Outcome of event
Event ID | OUTC COD |
---|---|
7583248 | OT |
Reactions reported
Event ID | PT |
---|---|
7583248 | CHEMOTHERAPY |
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 |
---|---|---|---|---|---|
7583248 | 1016903696 | 20090529 |