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
126605251 12660525 1 I 201607 20160730 20160817 20160817 PER US-CELGENEUS-USA-2016080102 CELGENE 72.54 YR M Y 99.88000 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
126605251 12660525 1 PS REVLIMID LENALIDOMIDE 1 Oral 25 MILLIGRAM N U 21880 25 MG CAPSULES
126605251 12660525 2 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown N U 0 UNKNOWN
126605251 12660525 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown 0 UNKNOWN
126605251 12660525 4 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126605251 12660525 1 Plasma cell myeloma
126605251 12660525 2 Product used for unknown indication
126605251 12660525 3 Product used for unknown indication
126605251 12660525 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126605251 12660525 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126605251 12660525 Oedema
126605251 12660525 Rash

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
126605251 12660525 1 20160610 20160729 0