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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6140954 | 6965795 | I | 6140954-9 | 20090317 | 20090331 | EXP | A-CH2009-24222 | ACTELION PHARMACEUTICALS US, INC. | F | N | 20090330 | MD | GERMANY |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6140954 | 1011367857 | PS | TRACLEER | 1 | ORAL | ORAL | D | D | 21290 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6140954 | 1011367857 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6140954 | HO |
Reactions reported
Event ID | PT |
---|---|
6140954 | BRONCHOPNEUMONIA |
6140954 | INFECTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6140954 | FGN |
6140954 | HP |
6140954 | OTH |
Therapies reported
no results found |