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
124203542 12420354 2 F 20160512 20160621 20160531 20160705 EXP FR-CELGENEUS-FRA-2016054340 CELGENE 57.26 YR F Y 88.00000 KG 20160705 OT FR FR

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
124203542 12420354 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U 21880 CAPSULES
124203542 12420354 2 SS APIXABAN APIXABAN 1 Unknown U U 0 2.5 MG UNKNOWN BID
124203542 12420354 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown Y U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124203542 12420354 1 Plasma cell myeloma
124203542 12420354 2 Plasma cell myeloma
124203542 12420354 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
124203542 12420354 HO
124203542 12420354 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124203542 12420354 Phlebitis
124203542 12420354 Thrombocytopenia

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
124203542 12420354 1 20151230 20160602 0
124203542 12420354 2 20151230 0
124203542 12420354 3 20151230 20160609 0