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
107343224 10734322 4 F 20110228 20160803 20150123 20160809 PER US-CELGENEUS-USA-2015010482 CELGENE 54.16 YR M Y 81.72000 KG 20160809 OT US US

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
107343224 10734322 1 PS REVLIMID LENALIDOMIDE 1 Oral 25 MILLIGRAM U U UNKNOWN 21880 25 MG CAPSULES
107343224 10734322 2 SS VELCADE BORTEZOMIB 1 Intravenous drip U U 66188 1.6 MG/M**2 INJECTION FOR INFUSION
107343224 10734322 3 SS DECADRON DEXAMETHASONE 1 Intravenous drip 1.6 MILLIGRAM/SQ. METER U U 0 40 MG INJECTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107343224 10734322 1 Plasma cell myeloma
107343224 10734322 2 Plasma cell myeloma
107343224 10734322 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
107343224 10734322 HO
107343224 10734322 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107343224 10734322 Anaemia
107343224 10734322 Back pain
107343224 10734322 Toxicity to various agents

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
107343224 10734322 1 20110222 20111025 0
107343224 10734322 2 20110222 20111214 0
107343224 10734322 3 20110222 20111214 0