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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126338152 | 12633815 | 2 | F | 20160615 | 20160825 | 20160808 | 20160831 | EXP | FR-TEVA-681378ACC | TEVA | 62.00 | YR | M | Y | 0.00000 | 20160831 | CN | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126338152 | 12633815 | 1 | PS | BENDAMUSTINE HYDROCHLORIDE. | BENDAMUSTINE HYDROCHLORIDE | 1 | Intravenous drip | 334 MILLIGRAM DAILY; | 668 | MG | Y | 22249 | 334 | MG | POWDER FOR INJECTION | QD | |||
| 126338152 | 12633815 | 2 | SS | MABTHERA | RITUXIMAB | 1 | Intravenous drip | U | 0 | 694.5 | MG | ||||||||
| 126338152 | 12633815 | 3 | C | KARDEGIC | ASPIRIN LYSINE | 1 | Unknown | 0 | |||||||||||
| 126338152 | 12633815 | 4 | C | ZELITREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 126338152 | 12633815 | 5 | C | INEXIUM /01479302/ | ESOMEPRAZOLE MAGNESIUM | 1 | Unknown | 0 | |||||||||||
| 126338152 | 12633815 | 6 | C | NEURONTIN | GABAPENTIN | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126338152 | 12633815 | 1 | Waldenstrom's macroglobulinaemia |
| 126338152 | 12633815 | 2 | Waldenstrom's macroglobulinaemia |
| 126338152 | 12633815 | 3 | Product used for unknown indication |
| 126338152 | 12633815 | 4 | Product used for unknown indication |
| 126338152 | 12633815 | 5 | Product used for unknown indication |
| 126338152 | 12633815 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126338152 | 12633815 | OT |
| 126338152 | 12633815 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126338152 | 12633815 | Acute kidney injury | |
| 126338152 | 12633815 | Drug reaction with eosinophilia and systemic symptoms | |
| 126338152 | 12633815 | 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 |
|---|---|---|---|---|---|---|
| 126338152 | 12633815 | 1 | 20160524 | 20160525 | 0 | |
| 126338152 | 12633815 | 2 | 20160524 | 20160524 | 0 |