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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126106042 | 12610604 | 2 | F | 20160724 | 20160726 | 20160801 | 20160803 | EXP | GB-AMGEN-GBRSP2016097172 | AMGEN | 47.00 | YR | A | F | Y | 0.00000 | 20160802 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126106042 | 12610604 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Unknown | 100 MUG (0.5 ML), UNK | U | 103951 | 100 | UG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||
126106042 | 12610604 | 2 | C | TACROLIMUS. | TACROLIMUS | 1 | Oral | 1 MG, UNK | 0 | 1 | MG | ||||||||
126106042 | 12610604 | 3 | C | PREDNISOLONE. | PREDNISOLONE | 1 | Oral | 1 MG, UNK | 0 | 1 | MG | ||||||||
126106042 | 12610604 | 4 | C | AZATHIOPRINE APS | 2 | Oral | 25 MG, UNK | 0 | 25 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126106042 | 12610604 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126106042 | 12610604 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126106042 | 12610604 | Infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |