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
117940113 11794011 3 F 201110 20160728 20151202 20160808 PER US-CELGENEUS-USA-2015103602 CELGENE 52.40 YR M Y 0.00000 20160808 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
117940113 11794011 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 25 MG CAPSULES
117940113 11794011 2 SS REVLIMID LENALIDOMIDE 1 Oral Y U UNKNOWN 21880 15 MG CAPSULES
117940113 11794011 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U U 0 40 MG CAPSULES

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117940113 11794011 1 Plasma cell myeloma
117940113 11794011 3 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117940113 11794011 Aggression
117940113 11794011 Decreased appetite
117940113 11794011 Dizziness
117940113 11794011 Drug intolerance
117940113 11794011 Fatigue
117940113 11794011 Headache
117940113 11794011 Nausea
117940113 11794011 Plasma cell myeloma
117940113 11794011 Rash

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
117940113 11794011 1 20110421 0
117940113 11794011 2 201106 20111010 0
117940113 11794011 3 20110421 20111010 0