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
127021281 12702128 1 I 20111014 20120109 20160831 20160831 PER US-CELGENEUS-163-21880-12010834 CELGENE 62.77 YR M Y 70.37000 KG 20160831 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
127021281 12702128 1 PS REVLIMID LENALIDOMIDE 1 Oral 25 MILLIGRAM U 21880 25 MG CAPSULES
127021281 12702128 2 SS DECADRON DEXAMETHASONE 1 Oral 1-4,9-12,17-20 TIMES 4 CYCLES THEN DAYS 1-4 U U 0 40 MG UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127021281 12702128 1 Plasma cell myeloma
127021281 12702128 2 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
127021281 12702128 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127021281 12702128 Hyperglycaemia
127021281 12702128 Hyponatraemia
127021281 12702128 Pain
127021281 12702128 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
127021281 12702128 1 20110926 20120109 0
127021281 12702128 2 20110926 20120109 0