Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126819151 | 12681915 | 1 | I | 20151221 | 20160824 | 20160824 | PER | US-ACTELION-A-US2015-129287 | ACTELION | 72.00 | YR | E | F | Y | 0.00000 | 20160824 | OT | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126819151 | 12681915 | 1 | PS | TRACLEER | BOSENTAN | 1 | Oral | UNK | IP060P0101, OP019P0101,OP026P0101 | 21290 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126819151 | 12681915 | 1 | Pulmonary arterial hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126819151 | 12681915 | Bronchitis | |
126819151 | 12681915 | Cough | |
126819151 | 12681915 | Dysphonia | |
126819151 | 12681915 | Head discomfort | |
126819151 | 12681915 | Headache | |
126819151 | 12681915 | Nasal congestion | |
126819151 | 12681915 | Nasopharyngitis | |
126819151 | 12681915 | Secretion discharge |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |