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
125217702 12521770 2 F 20160409 20160624 20160701 20160706 EXP GB-BAUSCH-BL-2016-015113 BAUSCH AND LOMB 0.00 M Y 0.00000 20160706 MD GB GB

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
125217702 12521770 1 PS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 40069
125217702 12521770 2 SS BORTEZOMIB BORTEZOMIB 1 Unknown 0
125217702 12521770 3 SS FARYDAK PANOBINOSTAT 1 Oral 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125217702 12521770 1 Plasma cell myeloma
125217702 12521770 2 Plasma cell myeloma
125217702 12521770 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125217702 12521770 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125217702 12521770 Infection
125217702 12521770 Malignant neoplasm progression
125217702 12521770 Plasma cell myeloma

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
125217702 12521770 1 20160409 0
125217702 12521770 2 20160409 0
125217702 12521770 3 20160409 0