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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125226631 | 12522663 | 1 | I | 2015 | 20160622 | 20160701 | 20160701 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201607000121 | ELI LILLY AND CO | 73.00 | YR | M | Y | 48.00000 | KG | 20160701 | CN | BR | BR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125226631 | 12522663 | 1 | PS | EFFIENT | PRASUGREL HYDROCHLORIDE | 1 | Oral | 10 MG, UNKNOWN | Y | 22307 | 10 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125226631 | 12522663 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125226631 | 12522663 | OT |
125226631 | 12522663 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125226631 | 12522663 | Constipation | |
125226631 | 12522663 | Myocardial infarction | |
125226631 | 12522663 | Nausea | |
125226631 | 12522663 | Sleep disorder | |
125226631 | 12522663 | Syncope |
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 |
---|---|---|---|---|---|---|
125226631 | 12522663 | 1 | 2015 | 2015 | 0 |