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
125718051 12571805 1 I 20160715 20160719 20160719 PER US-TAKEDA-2016MPI006473 TAKEDA 0.00 M Y 0.00000 20160719 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
125718051 12571805 1 PS VELCADE BORTEZOMIB 1 Unknown UNK U 21602 INJECTION
125718051 12571805 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U 0
125718051 12571805 3 SS REVLIMID LENALIDOMIDE 1 Oral 25 MG, QD 0 25 MG QD
125718051 12571805 4 SS REVLIMID LENALIDOMIDE 1 Oral 10 MG, QD 0 10 MG QD
125718051 12571805 5 SS REVLIMID LENALIDOMIDE 1 Oral 5 MG, UNK 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125718051 12571805 1 Product used for unknown indication
125718051 12571805 2 Product used for unknown indication
125718051 12571805 3 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125718051 12571805 Activities of daily living impaired
125718051 12571805 Euphoric mood
125718051 12571805 Fatigue
125718051 12571805 Gastrointestinal disorder
125718051 12571805 Neuropathy peripheral

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
125718051 12571805 1 200901 200903 0
125718051 12571805 2 200901 200903 0
125718051 12571805 3 200901 201003 0
125718051 12571805 4 201003 0
125718051 12571805 5 201407 0