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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125960181 | 12596018 | 1 | I | 20160516 | 20160726 | 20160726 | PER | US-AMGEN-USASL2016064455 | AMGEN | 50.00 | YR | A | M | Y | 0.00000 | 20160726 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125960181 | 12596018 | 1 | PS | KYPROLIS | CARFILZOMIB | 1 | Unknown | UNK | U | 202714 | UNKNOWN FORMULATION | ||||||||
| 125960181 | 12596018 | 2 | SS | DECADRON | DEXAMETHASONE | 1 | Unknown | 40 MG, QD | 0 | 40 | MG | QD | |||||||
| 125960181 | 12596018 | 3 | SS | DECADRON | DEXAMETHASONE | 1 | Unknown | 4 MG, UNK | 0 | 4 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125960181 | 12596018 | 1 | Product used for unknown indication |
| 125960181 | 12596018 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125960181 | 12596018 | Headache | |
| 125960181 | 12596018 | Malaise | |
| 125960181 | 12596018 | Nausea | |
| 125960181 | 12596018 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |