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
127631012 12763101 2 F 20151112 20160922 20160920 20160930 PER US-CELGENEUS-USA-2016093592 CELGENE 75.27 YR F Y 53.89000 KG 20160930 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
127631012 12763101 1 PS REVLIMID LENALIDOMIDE 1 Oral 5 MILLIGRAM U U UNKNOWN 21880 5 MG CAPSULES
127631012 12763101 2 SS VELCADE BORTEZOMIB 1 Subcutaneous U U 66188 INJECTION /wk
127631012 12763101 3 SS VELCADE BORTEZOMIB 1 Subcutaneous U U 66188 INJECTION /wk
127631012 12763101 4 SS DECADRON DEXAMETHASONE 1 Oral U U 0 UNKNOWN
127631012 12763101 5 SS ZOMETA ZOLEDRONIC ACID 1 Intravenous drip U U 0 4 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127631012 12763101 1 Plasma cell myeloma
127631012 12763101 2 Plasma cell myeloma
127631012 12763101 4 Plasma cell myeloma
127631012 12763101 5 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
127631012 12763101 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127631012 12763101 Nausea
127631012 12763101 Vomiting

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
127631012 12763101 1 20140620 20150201 0
127631012 12763101 2 20010808 20140808 0
127631012 12763101 3 20140727 20141024 0
127631012 12763101 4 20140627 20141024 0
127631012 12763101 5 20140618 20160105 0