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
124148102 12414810 2 F 20160201 20160627 20160529 20160704 EXP PHHY2016IT073077 NOVARTIS 84.94 YR F Y 0.00000 20160704 OT IT IT

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
124148102 12414810 1 PS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) UNK Y 21223 SOLUTION FOR INJECTION
124148102 12414810 2 C CANDESARTAN CANDESARTAN 1 Unknown U 0
124148102 12414810 3 C ATORVASTATIN ATORVASTATIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124148102 12414810 1 Metastases to bone
124148102 12414810 2 Product used for unknown indication
124148102 12414810 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124148102 12414810 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124148102 12414810 Bone lesion
124148102 12414810 Exposed bone in jaw
124148102 12414810 Gingival erythema
124148102 12414810 Osteonecrosis of jaw
124148102 12414810 Swelling

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
124148102 12414810 1 20120101 20160201 0