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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126277633 | 12627763 | 3 | F | 20160809 | 20160806 | 20160817 | PER | PHEH2016US019433 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160817 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126277633 | 12627763 | 1 | PS | PROMACTA | ELTROMBOPAG OLAMINE | 1 | Oral | 50 MG, QD | Y | U | 22291 | 50 | MG | TABLET | QD | ||||
126277633 | 12627763 | 2 | SS | PROMACTA | ELTROMBOPAG OLAMINE | 1 | Oral | 25 MG, QD | Y | U | 22291 | 25 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126277633 | 12627763 | 1 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126277633 | 12627763 | Abdominal distension | |
126277633 | 12627763 | Diarrhoea | |
126277633 | 12627763 | Diplopia | |
126277633 | 12627763 | Splenomegaly |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |