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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122698082 | 12269808 | 2 | F | 20160411 | 20160916 | 20160415 | 20160922 | PER | PHEH2016US009173 | NOVARTIS | 52.78 | YR | F | Y | 0.00000 | 20160922 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122698082 | 12269808 | 1 | PS | PROMACTA | ELTROMBOPAG OLAMINE | 1 | Oral | 50 MG, UNK | N | 22291 | 50 | MG | TABLET | ||||||
122698082 | 12269808 | 2 | SS | PROMACTA | ELTROMBOPAG OLAMINE | 1 | Oral | 25 MG, UNK | N | 22291 | 25 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122698082 | 12269808 | 1 | Thrombocytopenia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122698082 | 12269808 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122698082 | 12269808 | Fatigue | |
122698082 | 12269808 | Insomnia | |
122698082 | 12269808 | Platelet count decreased |
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 |
---|---|---|---|---|---|---|
122698082 | 12269808 | 1 | 20150420 | 0 | ||
122698082 | 12269808 | 2 | 20160822 | 0 |