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
125950971 12595097 1 I 20160719 20160726 20160726 PER US-TAKEDA-2016MPI006577 TAKEDA 89.00 YR M Y 0.00000 20160726 CN 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
125950971 12595097 1 PS VELCADE BORTEZOMIB 1 Subcutaneous 2.5 MG, 1/WEEK U 21602 2.5 MG INJECTION /wk
125950971 12595097 2 C HYDROCODONE HYDROCODONE 1 Unknown 10 MG, UNK U 0 10 MG
125950971 12595097 3 C ELIQUIS APIXABAN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125950971 12595097 1 Mantle cell lymphoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125950971 12595097 Arthralgia
125950971 12595097 Back pain
125950971 12595097 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
125950971 12595097 1 20160715 0