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
121801813 12180181 3 F 20151113 20160810 20160315 20160817 PER US-CELGENEUS-USA-2016033033 CELGENE 73.02 YR M Y 97.61000 KG 20160817 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
121801813 12180181 1 PS REVLIMID LENALIDOMIDE 1 Oral 15 MILLIGRAM U UNKNOWN 21880 15 MG CAPSULES QOD
121801813 12180181 2 SS VELCADE BORTEZOMIB 1 Subcutaneous U 66188 1.3 MG/M**2 INJECTION /wk
121801813 12180181 3 SS PREDNISONE. PREDNISONE 1 Oral 1.3 MILLIGRAM/SQ. METER U 66188 40 MG UNKNOWN /wk
121801813 12180181 4 C RBC HUMAN RED BLOOD CELL 1 Intravenous drip 40 MILLIGRAM 0 INJECTION
121801813 12180181 5 C LASIX FUROSEMIDE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121801813 12180181 1 Plasma cell myeloma
121801813 12180181 2 Plasma cell myeloma
121801813 12180181 3 Plasma cell myeloma
121801813 12180181 4 Transfusion
121801813 12180181 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121801813 12180181 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121801813 12180181 Acute respiratory failure
121801813 12180181 Anaemia

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
121801813 12180181 1 20151110 0
121801813 12180181 2 20151110 0
121801813 12180181 3 20151110 0