The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
91759052 9175905 2 F 20130228 20130313 20130320 20160929 EXP GB-009507513-1303GBR007640 MERCK 47.00 YR M Y 63.00000 KG 20160929 OT GB GB

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
91759052 9175905 1 PS VORINOSTAT VORINOSTAT 1 Oral 300 MG, DAY 1-7 AND 15-21 N 21991 300 MG CAPSULE
91759052 9175905 2 SS DEXAMETHASONE TABLETS BP 2.0MG DEXAMETHASONE 1 Oral 20 MG, DAYS 1-4 AND 12-15 U 0 20 MG TABLET
91759052 9175905 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 500 MG, DAYS 1, 8, 15 U 0 500 MG TABLET
91759052 9175905 4 SS THALIDOMIDE THALIDOMIDE 1 Oral 100 MG, DAILY FOR 21 DAYS U 0 100 MG CAPSULE
91759052 9175905 5 SS LENALIDOMIDE LENALIDOMIDE 1 Oral 10 MG, DAY 1-7 AND 15-21 N 0 10 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91759052 9175905 1 Plasma cell myeloma
91759052 9175905 2 Plasma cell myeloma
91759052 9175905 3 Plasma cell myeloma
91759052 9175905 5 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
91759052 9175905 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
91759052 9175905 Nodule

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
91759052 9175905 1 20130110 0
91759052 9175905 2 20120321 0
91759052 9175905 3 20120321 0
91759052 9175905 4 20120321 0
91759052 9175905 5 20130110 0