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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124795612 | 12479561 | 2 | F | 20160517 | 20160818 | 20160620 | 20160823 | EXP | DK-DKMA-WBS-0003763 | DK-ROCHE-1778159 | ROCHE | 58.60 | YR | M | Y | 75.50000 | KG | 20160823 | PH | DK | DK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124795612 | 12479561 | 1 | PS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | U | HAVES IKKE | 103705 | 750 | MG | SOLUTION FOR INFUSION | QD | |||||
| 124795612 | 12479561 | 2 | C | ARANESP | DARBEPOETIN ALFA | 1 | Unknown | 0 | |||||||||||
| 124795612 | 12479561 | 3 | C | BERODUAL | FENOTEROL HYDROBROMIDEIPRATROPIUM BROMIDE | 1 | Unknown | 0 | |||||||||||
| 124795612 | 12479561 | 4 | C | FURIX | FUROSEMIDE | 1 | Unknown | 0 | |||||||||||
| 124795612 | 12479561 | 5 | C | HJERTEMAGNYL | ASPIRINMAGNESIUM OXIDE | 1 | Unknown | 0 | |||||||||||
| 124795612 | 12479561 | 6 | C | KALEORID | POTASSIUM CHLORIDE | 1 | Unknown | 0 | |||||||||||
| 124795612 | 12479561 | 7 | C | NIVESTIM | FILGRASTIM | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124795612 | 12479561 | 1 | Epstein-Barr virus infection |
| 124795612 | 12479561 | 2 | Anaemia |
| 124795612 | 12479561 | 3 | Bronchospasm |
| 124795612 | 12479561 | 4 | Diuretic therapy |
| 124795612 | 12479561 | 5 | Thrombosis prophylaxis |
| 124795612 | 12479561 | 6 | Mineral supplementation |
| 124795612 | 12479561 | 7 | Neutropenia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124795612 | 12479561 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124795612 | 12479561 | Hepatic failure | |
| 124795612 | 12479561 | Off label use |
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 |
|---|---|---|---|---|---|---|
| 124795612 | 12479561 | 1 | 20160505 | 20160505 | 0 |