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
119360112 11936011 2 F 2015 20160202 20160121 20160726 PER US-AMGEN-USASL2015113262 AMGEN 65.00 YR E F 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
119360112 11936011 1 PS KYPROLIS CARFILZOMIB 1 Unknown UNK U 202714 INTRAVENOUS INFUSION
119360112 11936011 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 20 MG, UNK 0 20 MG TABLET
119360112 11936011 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) UNK 0 TABLET
119360112 11936011 4 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119360112 11936011 1 Plasma cell myeloma
119360112 11936011 2 Product used for unknown indication
119360112 11936011 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119360112 11936011 Constipation
119360112 11936011 Diarrhoea
119360112 11936011 Disorientation
119360112 11936011 Feeling abnormal
119360112 11936011 Hypoacusis
119360112 11936011 Incorrect dose administered
119360112 11936011 Increased appetite
119360112 11936011 Insomnia
119360112 11936011 Malaise
119360112 11936011 Nasopharyngitis
119360112 11936011 Nausea
119360112 11936011 Speech disorder
119360112 11936011 Unevaluable event

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
119360112 11936011 1 20150721 0