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
119360904 11936090 4 F 201601 20160707 20160121 20160712 EXP US-AMGEN-USASL2015133135 AMGEN 71.00 YR E M Y 0.00000 20160712 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
119360904 11936090 1 PS KYPROLIS CARFILZOMIB 1 Unknown UNK U 202714 INTRAVENOUS INFUSION
119360904 11936090 2 SS KYPROLIS CARFILZOMIB 1 Unknown UNK U 202714 INTRAVENOUS INFUSION
119360904 11936090 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 4 MG, TOOK 10 TABLETS AT 4MG /HE TAKES 20 ON ONE DAY AND 20 THE NEXT 0 4 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119360904 11936090 1 Product used for unknown indication
119360904 11936090 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119360904 11936090 OT
119360904 11936090 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119360904 11936090 Asthenia
119360904 11936090 Blood glucose increased
119360904 11936090 Clostridium difficile infection
119360904 11936090 Hospice care
119360904 11936090 Night sweats
119360904 11936090 Pneumonia
119360904 11936090 Rehabilitation therapy
119360904 11936090 Walking aid user

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
119360904 11936090 2 20160225 201603 0