The Safety Rates Drug Report

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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
125961511 12596151 1 I 2016 20160404 20160726 20160726 PER US-AMGEN-USASL2016042910 AMGEN 59.00 YR A 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
125961511 12596151 1 PS KYPROLIS CARFILZOMIB 1 Unknown THURSDAY AND FRIDAY U 202714 INTRAVENOUS INFUSION
125961511 12596151 2 SS DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Unknown UNK 0
125961511 12596151 3 SS FENTANYL. FENTANYL 1 Unknown 125 MUG 0 125 UG
125961511 12596151 4 SS FENTANYL. FENTANYL 1 Unknown 100 MUG, UNK 0 100 UG
125961511 12596151 5 C GABAPENTIN. GABAPENTIN 1 100 MG, UNK 0 100 MG
125961511 12596151 6 C MORPHINE MORPHINE 1 4 MG, UNK 0 4 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125961511 12596151 1 Plasma cell myeloma
125961511 12596151 2 Product used for unknown indication
125961511 12596151 3 Pain
125961511 12596151 5 Pain
125961511 12596151 6 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125961511 12596151 Hypersomnia
125961511 12596151 Somnolence

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
125961511 12596151 1 20160331 0