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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
104329843 | 10432984 | 3 | F | 20140821 | 20160926 | 20140905 | 20160930 | EXP | DE-TEVA-505637USA | TEVA | 0.00 | M | Y | 0.00000 | 20161001 | MD | DE | DE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
104329843 | 10432984 | 1 | PS | BENDAMUSTINE HYDROCHLORIDE. | BENDAMUSTINE HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | UNK UNK, UNKNOWN FREQ. | D | 22249 | POWDER FOR INJECTION | ||||||||
104329843 | 10432984 | 2 | SS | RITUXIMAB | RITUXIMAB | 1 | Intravenous (not otherwise specified) | UNK, UNKNOWN FREQ. | D | 0 | |||||||||
104329843 | 10432984 | 3 | SS | RITUXIMAB | RITUXIMAB | 1 | Subcutaneous | UNK UNK, UNKNOWN FREQ. | D | 0 | |||||||||
104329843 | 10432984 | 4 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | UNK UNK, UNKNOWN FREQ. | D | 89081 | |||||||||
104329843 | 10432984 | 5 | C | MORPHINE | MORPHINE | 1 | Unknown | 2 ML, PER HOUR | U | 0 | 2 | ML | |||||||
104329843 | 10432984 | 6 | C | OXYGEN. | OXYGEN | 1 | Unknown | 12 L, PER MIN | U | 0 | 12 | L |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
104329843 | 10432984 | 1 | B-cell lymphoma |
104329843 | 10432984 | 2 | B-cell lymphoma |
104329843 | 10432984 | 3 | B-cell lymphoma |
104329843 | 10432984 | 4 | Product used for unknown indication |
104329843 | 10432984 | 5 | Product used for unknown indication |
104329843 | 10432984 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
104329843 | 10432984 | DE |
104329843 | 10432984 | HO |
104329843 | 10432984 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
104329843 | 10432984 | General physical health deterioration | |
104329843 | 10432984 | Pneumonia | |
104329843 | 10432984 | Pulmonary oedema |
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 |
---|---|---|---|---|---|---|
104329843 | 10432984 | 1 | 20140805 | 0 | ||
104329843 | 10432984 | 2 | 20140801 | 0 | ||
104329843 | 10432984 | 3 | 20140804 | 0 | ||
104329843 | 10432984 | 4 | 20140728 | 0 | ||
104329843 | 10432984 | 5 | 20140822 | 20140822 | 0 | |
104329843 | 10432984 | 6 | 20140822 | 20140822 | 0 |