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
119359982 11935998 2 F 2015 20160225 20160121 20160726 PER US-AMGEN-USASP2015115858 AMGEN 65.00 YR E M Y 0.00000 20160726 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
119359982 11935998 1 PS KYPROLIS CARFILZOMIB 1 Unknown UNK, UNK U 202714 INTRAVENOUS INFUSION
119359982 11935998 2 SS THALIDOMIDE THALIDOMIDE 1 Unknown UNK 0
119359982 11935998 3 C REVLIMID LENALIDOMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119359982 11935998 1 Plasma cell myeloma
119359982 11935998 2 Product used for unknown indication
119359982 11935998 3 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119359982 11935998 Activities of daily living impaired
119359982 11935998 Asthenia
119359982 11935998 Fatigue
119359982 11935998 Frustration tolerance decreased
119359982 11935998 Mobility decreased
119359982 11935998 Muscle spasms
119359982 11935998 Pain in extremity

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
119359982 11935998 1 201510 0