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
121665962 12166596 2 F 20151130 20160810 20160309 20160815 PER US-CELGENEUS-USA-2016031655 CELGENE 65.63 YR M Y 60.75000 KG 20160815 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
121665962 12166596 1 PS POMALYST POMALIDOMIDE 1 Oral 4 MILLIGRAM U U UNKNOWN 204026 4 MG CAPSULES QD
121665962 12166596 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U U UNKNOWN 204026 40 MG CAPSULES /wk
121665962 12166596 3 C ZOMETA ZOLEDRONIC ACID 1 Unknown 0 UNKNOWN
121665962 12166596 4 C MS CONTIN MORPHINE SULFATE 1 Unknown 0 UNKNOWN
121665962 12166596 5 C Oxycodone OXYCODONE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121665962 12166596 1 Plasma cell myeloma
121665962 12166596 2 Plasma cell myeloma
121665962 12166596 3 Renal failure
121665962 12166596 4 Product used for unknown indication
121665962 12166596 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121665962 12166596 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121665962 12166596 Acute kidney injury
121665962 12166596 Constipation

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
121665962 12166596 1 20151108 20151128 0
121665962 12166596 2 20151108 20151122 0
121665962 12166596 3 20151120 0
121665962 12166596 4 20151119 0
121665962 12166596 5 20151119 0