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
126110972 12611097 2 F 201512 20160921 20160801 20160927 PER US-CELGENEUS-USA-2016077451 CELGENE 85.46 YR M Y 0.00000 20160927 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
126110972 12611097 1 PS POMALYST POMALIDOMIDE 1 Oral 4 MILLIGRAM U UNKNOWN 204026 4 MG CAPSULES
126110972 12611097 2 SS DECADRON DEXAMETHASONE 1 Unknown U U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126110972 12611097 1 Plasma cell myeloma
126110972 12611097 2 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126110972 12611097 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126110972 12611097 Abdominal distension
126110972 12611097 Abdominal pain
126110972 12611097 Clostridium difficile infection
126110972 12611097 Muscular weakness
126110972 12611097 Pneumonia

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
126110972 12611097 1 20150619 0