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
126255041 12625504 1 I 20160721 20160805 20160805 EXP AU-CELGENEUS-AUS-2016075302 CELGENE 0.00 Y 0.00000 20160805 MD AU AU

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
126255041 12625504 1 PS REVLIMID LENALIDOMIDE 1 Oral U U 21880 10 MG CAPSULES QD
126255041 12625504 2 SS REVLIMID LENALIDOMIDE 1 Oral U U 21880 15 MG CAPSULES QD
126255041 12625504 3 SS PREDNISOLONE. PREDNISOLONE 1 Unknown 250 MILLIGRAM U U 0 500 MG UNKNOWN QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126255041 12625504 1 Plasma cell myeloma
126255041 12625504 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126255041 12625504 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126255041 12625504 Acute myeloid leukaemia
126255041 12625504 Anaemia
126255041 12625504 Bone marrow failure
126255041 12625504 Diarrhoea
126255041 12625504 Fatigue
126255041 12625504 Gastrointestinal carcinoma
126255041 12625504 Hyperglycaemia
126255041 12625504 Insomnia
126255041 12625504 Lower respiratory tract infection
126255041 12625504 Muscle spasms
126255041 12625504 Neuropathy peripheral
126255041 12625504 Neutropenia
126255041 12625504 Retinal vein thrombosis
126255041 12625504 Skin cancer
126255041 12625504 Thrombocytopenia
126255041 12625504 Upper respiratory tract infection
126255041 12625504 Varicella zoster virus infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found