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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125215081 | 12521508 | 1 | I | 20160604 | 20160625 | 20160701 | 20160701 | EXP | CO-AMGEN-COLSL2016084375 | AMGEN | 87.00 | YR | E | F | Y | 0.00000 | 20160701 | OT | CO | CO |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125215081 | 12521508 | 1 | PS | PROLIA | DENOSUMAB | 1 | Subcutaneous | 60 MUG, Q6MO | 125320 | 60 | UG | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125215081 | 12521508 | 1 | Osteoporosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125215081 | 12521508 | DE |
125215081 | 12521508 | OT |
125215081 | 12521508 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125215081 | 12521508 | Cardio-respiratory arrest | |
125215081 | 12521508 | Hospitalisation |
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 |
---|---|---|---|---|---|---|
125215081 | 12521508 | 1 | 20150630 | 20160213 | 0 |