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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126458181 | 12645818 | 1 | I | 201512 | 20160223 | 20160811 | 20160811 | PER | US-ENDO PHARMACEUTICALS INC.-2016-001810 | ENDO | 77.02 | YR | F | Y | 108.96000 | KG | 20160811 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126458181 | 12645818 | 1 | PS | PREDNISONE TABLETS | PREDNISONE | 1 | Oral | 40256 | 5 | MG | TABLETS | QD | |||||||
126458181 | 12645818 | 2 | SS | PREDNISONE TABLETS | PREDNISONE | 1 | Oral | 40256 | 30 | MG | TABLETS | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126458181 | 12645818 | 1 | Rheumatoid arthritis |
126458181 | 12645818 | 2 | Pain in extremity |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126458181 | 12645818 | Cough |
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 |
---|---|---|---|---|---|---|
126458181 | 12645818 | 1 | 2013 | 201601 | 0 | |
126458181 | 12645818 | 2 | 20160129 | 0 |