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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126664771 | 12666477 | 1 | I | 20160811 | 20160819 | 20160819 | EXP | GB-AMGEN-GBRSL2016105799 | AMGEN | 0.00 | F | Y | 0.00000 | 20160818 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126664771 | 12666477 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Unknown | 50 MUG, UNK | U | 103951 | 50 | UG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126664771 | 12666477 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126664771 | 12666477 | HO |
126664771 | 12666477 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126664771 | 12666477 | Atypical pneumonia | |
126664771 | 12666477 | Hypotension | |
126664771 | 12666477 | Oedema peripheral |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |