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
71346655 7134665 5 F 20090722 20160808 20090930 20160818 EXP US-CELGENEUS-163-21880-09081314 CELGENE 62.97 YR M Y 0.00000 20160818 MD 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
71346655 7134665 1 PS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 25 MG CAPSULES QD
71346655 7134665 2 SS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 25 MG CAPSULES
71346655 7134665 3 SS ZOMETA ZOLEDRONIC ACID 1 Unknown Y U 0 UNKNOWN
71346655 7134665 4 C Regular Aspirin ASPIRIN 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
71346655 7134665 1 Plasma cell myeloma
71346655 7134665 3 Product used for unknown indication
71346655 7134665 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
71346655 7134665 OT
71346655 7134665 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
71346655 7134665 Migraine
71346655 7134665 Osteonecrosis of jaw

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
71346655 7134665 1 20081021 0
71346655 7134665 2 20090108 0
71346655 7134665 3 200504 200905 0