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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126122041 | 12612204 | 1 | I | 20150701 | 20160722 | 20160801 | 20160801 | EXP | PHHY2016IT102796 | SANDOZ | 72.66 | YR | F | Y | 61.00000 | KG | 20160801 | OT | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126122041 | 12612204 | 1 | PS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Oral | 20 MG, QD | Y | 77087 | 20 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126122041 | 12612204 | 1 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126122041 | 12612204 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126122041 | 12612204 | Abdominal pain | |
126122041 | 12612204 | Diarrhoea | |
126122041 | 12612204 | Erythema | |
126122041 | 12612204 | Osteoarthritis | |
126122041 | 12612204 | Rash pustular | |
126122041 | 12612204 | Tachycardia |
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 |
---|---|---|---|---|---|---|
126122041 | 12612204 | 1 | 20150701 | 20151031 | 0 |