The Safety Rates Drug Report

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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
124867213 12486721 3 F 2016 20160826 20160621 20160907 PER US-CELGENEUS-USA-2016053430 CELGENE 0.00 F Y 76.27000 KG 20160907 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
124867213 12486721 1 PS REVLIMID LENALIDOMIDE 1 Oral 10 MILLIGRAM U A2115A 21880 10 MG CAPSULES
124867213 12486721 2 SS VELCADE BORTEZOMIB 1 Subcutaneous U U 0 3.5 MG INJECTION
124867213 12486721 3 C Potassium POTASSIUM 1 Unknown 595(99) 0 UNKNOWN
124867213 12486721 4 C LASIX FUROSEMIDE 1 Oral 0 20 MG TABLETS
124867213 12486721 5 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown 0 20 MG UNKNOWN /wk
124867213 12486721 6 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown 0 4 MG UNKNOWN
124867213 12486721 7 C PREDNISONE. PREDNISONE 1 Unknown 0 5 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124867213 12486721 1 Plasma cell myeloma
124867213 12486721 2 Plasma cell myeloma
124867213 12486721 3 Product used for unknown indication
124867213 12486721 4 Product used for unknown indication
124867213 12486721 5 Plasma cell myeloma
124867213 12486721 7 Polymyalgia rheumatica

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124867213 12486721 Deafness
124867213 12486721 Diarrhoea
124867213 12486721 Dizziness
124867213 12486721 Muscle spasms
124867213 12486721 Tremor

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
124867213 12486721 1 20160312 0
124867213 12486721 2 201606 0
124867213 12486721 5 201607 0