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
126439811 12643981 1 I 20130902 20131111 20160811 20160811 PER US-CELGENEUS-163-21880-13112399 CELGENE 62.03 YR F Y 61.93000 KG 20160811 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
126439811 12643981 1 PS REVLIMID LENALIDOMIDE 1 Oral 10 MILLIGRAM U 21880 10 MG CAPSULES QD
126439811 12643981 2 SS BORTEZOMIB BORTEZOMIB 1 Subcutaneous U U 0 1.3 MG/M**2 INJECTION
126439811 12643981 3 SS DECADRON DEXAMETHASONE 1 Oral U U 0 40 MG TABLETS /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126439811 12643981 1 Plasma cell myeloma
126439811 12643981 2 Plasma cell myeloma
126439811 12643981 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126439811 12643981 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126439811 12643981 Anaemia
126439811 12643981 Dehydration
126439811 12643981 Leukopenia
126439811 12643981 Systemic inflammatory response syndrome

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
126439811 12643981 1 20130731 20131028 0
126439811 12643981 2 20130731 20131028 0
126439811 12643981 3 20130731 20131111 0