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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126789262 | 12678926 | 2 | F | 20160830 | 20160824 | 20160906 | EXP | RU-ROCHE-1819057 | ROCHE | , LORIE Y, ZVONKOV E, GEMDJIAN E, MAGOMEDOVA A, MELIKYAN A, MANGASAROVA J, GRIBANOVA E, ZHEREBTSOVA V, KRAVCHENKO S AND SAVCHENKO V INTENSIVE INDUCTION, AUTOLOGOUS STEM CELL TRANSPLANTATION AND RITUXIMAB MAINTENANCE HAS CHANGED EVENT FREE SURVIVAL AND OVERALL SURVIVAL IN MANTLE CELL LYMPHOMA PATIENTS USING GEMCITABINE AND OXALIPLATIN IN FIRST LINE THERAPY.. BLOOD: 54TH ANNUAL MEETING OF THE AMERICAN SOCIETY OF HEMATOLOGY, ASH, 2012 2012;120(21):-. | 0.00 | Y | 0.00000 | 20160906 | MD | RU | RU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126789262 | 12678926 | 1 | PS | Rituximab | RITUXIMAB | 1 | Intravenous (not otherwise specified) | ON DAY 1 | U | 103705 | 375 | MG/M**2 | SOLUTION FOR INFUSION | ||||||
126789262 | 12678926 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 1000 MG/SQ.M/DAY ON DAY 2 | U | 0 | |||||||||
126789262 | 12678926 | 3 | SS | CYTARABINE. | CYTARABINE | 1 | Unknown | ON DAYS 3-4 | U | 0 | 3000 | MG/M**2 | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126789262 | 12678926 | 1 | Mantle cell lymphoma |
126789262 | 12678926 | 2 | Mantle cell lymphoma |
126789262 | 12678926 | 3 | Mantle cell lymphoma |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126789262 | 12678926 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126789262 | 12678926 | Acute kidney injury | |
126789262 | 12678926 | Septic shock |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |