The Safety Rates Drug Report

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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
127600081 12760008 1 I 20160905 20160919 20160919 EXP PE-TEVA-693018ISR TEVA CHAVEZ JFV, MENDOZA RER, LLERENA KMA, VALENCIA F, ENRIQUEZ D, PALACIOS V, ET AL. CYCLOPHOSPHAMIDE, THALIDOMIDE AND DEXAMETHASONE (CTD) AS INITIAL THERAPY FOR NEWLY DIAGNOSED MULTIPLE MYELOMA PATIENTS. J-CLIN-ONCOL 2016;34 (SUPPL.)(15): ABSTR. 8051. 76.00 YR Y 0.00000 20160919 OT PE PE

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
127600081 12760008 1 PS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 40MG WEEKLY; 28-DAY CYCLE U 80968
127600081 12760008 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 400MG/M2 FOR 5 DAYS; 28-DAY CYCLE U 0
127600081 12760008 3 SS thalidomide THALIDOMIDE 1 Unknown 100MG/DAY; 28-DAY CYCLE U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127600081 12760008 1 Plasma cell myeloma
127600081 12760008 2 Plasma cell myeloma
127600081 12760008 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
127600081 12760008 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127600081 12760008 Death

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found