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
125721101 12572110 1 I 20160301 20160715 20160719 20160719 EXP GB-MHRA-EYC 00142289 PHFR2016GB005851 NOVARTIS 76.00 YR F Y 0.00000 20160719 OT 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
125721101 12572110 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4 MG, UNK U UNKNOWN 21223 4 MG SOLUTION FOR INJECTION
125721101 12572110 2 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown U 0
125721101 12572110 3 C DEXAMETASON DEXAMETHASONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125721101 12572110 1 Plasma cell myeloma
125721101 12572110 2 Product used for unknown indication
125721101 12572110 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125721101 12572110 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125721101 12572110 Osteonecrosis of jaw

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
125721101 12572110 1 20140801 0