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
115894303 11589430 3 F 20150921 20160711 20151002 20160714 PER US-CELGENEUS-USA-2015095732 CELGENE 54.28 YR M Y 84.54000 KG 20160714 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
115894303 11589430 1 PS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 10 MG CAPSULES QOD
115894303 11589430 2 SS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 25 MG CAPSULES
115894303 11589430 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U UNKNOWN 21880 40 MG UNKNOWN /wk
115894303 11589430 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U UNKNOWN 21880 40 MG UNKNOWN /wk
115894303 11589430 5 SS VELCADE BORTEZOMIB 1 Subcutaneous U UNKNOWN 21880 1.3 MG/M**2 UNKNOWN
115894303 11589430 6 C DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Intravenous drip 0 INJECTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115894303 11589430 1 Plasma cell myeloma
115894303 11589430 3 Plasma cell myeloma
115894303 11589430 5 Plasma cell myeloma
115894303 11589430 6 Pain

Outcome of event

Event ID CASEID OUTC COD
115894303 11589430 DE
115894303 11589430 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115894303 11589430 Abdominal pain
115894303 11589430 Death

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
115894303 11589430 1 20150427 0
115894303 11589430 2 20150504 20150924 0
115894303 11589430 3 20150427 0
115894303 11589430 4 20150504 20150924 0
115894303 11589430 5 20150504 20150727 0