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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126103385 | 12610338 | 5 | F | 20160818 | 20160801 | 20160825 | EXP | US-GLAXOSMITHKLINE-US2016102479 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160825 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126103385 | 12610338 | 1 | SS | Ambrisentan | AMBRISENTAN | 1 | Unknown | 10 MG, QD | 1509507A | 0 | 10 | MG | TABLET | QD | |||||
126103385 | 12610338 | 2 | PS | VELETRI | EPOPROSTENOL | 1 | Unknown | UNK | Y | 20444 | |||||||||
126103385 | 12610338 | 3 | SS | ADCIRCA | TADALAFIL | 1 | Unknown | 20 MG, QD | U | 0 | 20 | MG | TABLET | QD | |||||
126103385 | 12610338 | 4 | SS | ADCIRCA | TADALAFIL | 1 | Unknown | 40 MG, QD | U | 0 | 40 | MG | TABLET | QD | |||||
126103385 | 12610338 | 5 | C | UPTRAVI | SELEXIPAG | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126103385 | 12610338 | 1 | Product used for unknown indication |
126103385 | 12610338 | 2 | Product used for unknown indication |
126103385 | 12610338 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126103385 | 12610338 | OT |
126103385 | 12610338 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126103385 | 12610338 | Flushing | |
126103385 | 12610338 | Oxygen consumption increased | |
126103385 | 12610338 | Pulmonary arterial hypertension | |
126103385 | 12610338 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
126103385 | 12610338 | 1 | 20160621 | 0 |