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
127633032 12763303 2 F 20160914 20160920 20160923 EXP US-CELGENEUS-USA-2016093747 CELGENE 0.00 F Y 69.01000 KG 20160923 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
127633032 12763303 1 PS REVLIMID LENALIDOMIDE 1 Oral U A2135B 21880 25 MG CAPSULES QD
127633032 12763303 2 SS REVLIMID LENALIDOMIDE 1 Oral U A2135B 21880 15 MG CAPSULES QD
127633032 12763303 3 SS REVLIMID LENALIDOMIDE 1 Oral U A2135B 21880 10 MG CAPSULES
127633032 12763303 4 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown U U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127633032 12763303 1 Plasma cell myeloma
127633032 12763303 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127633032 12763303 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127633032 12763303 Generalised oedema
127633032 12763303 Glaucoma
127633032 12763303 Muscle spasms
127633032 12763303 Musculoskeletal chest pain
127633032 12763303 Myalgia
127633032 12763303 Pulmonary congestion

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
127633032 12763303 1 20150415 0
127633032 12763303 2 201506 0
127633032 12763303 3 201609 0