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
126036781 12603678 1 I 20160202 20160715 20160728 20160728 EXP GB-BAUSCH-BL-2016-017526 BAUSCH AND LOMB 72.00 YR F Y 69.00000 KG 20160728 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
126036781 12603678 1 PS PREDNISOLONE. PREDNISOLONE 1 Oral 40070
126036781 12603678 2 SS MELPHALAN MELPHALAN 1 Oral 0
126036781 12603678 3 SS VELCADE BORTEZOMIB 1 Subcutaneous 0 2.15 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126036781 12603678 1 Plasma cell myeloma
126036781 12603678 2 Plasma cell myeloma
126036781 12603678 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126036781 12603678 HO
126036781 12603678 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126036781 12603678 Confusional state
126036781 12603678 Dehydration
126036781 12603678 Dyspnoea
126036781 12603678 Nausea
126036781 12603678 Neutropenia
126036781 12603678 Rash
126036781 12603678 Rash macular
126036781 12603678 Sepsis

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
126036781 12603678 1 20160202 20160205 0
126036781 12603678 2 20160202 20160205 0
126036781 12603678 3 20160202 20160209 0