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
121431553 12143155 3 F 2015 20160627 20160303 20160701 EXP PHHY2016AT026091 NOVARTIS 72.00 YR F Y 0.00000 20160702 CN AT AT

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
121431553 12143155 1 PS ACLASTA ZOLEDRONIC ACID 1 Unknown ANNUALLY 21817 SOLUTION FOR INJECTION
121431553 12143155 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
121431553 12143155 3 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
121431553 12143155 4 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
121431553 12143155 5 C OLEOVIT 2 Unknown UNK UNK, QW U 0 /wk
121431553 12143155 6 C CALCIUM CALCIUM 1 Unknown UNK UNK, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121431553 12143155 1 Product used for unknown indication
121431553 12143155 5 Calcium deficiency
121431553 12143155 6 Calcium deficiency

Outcome of event

Event ID CASEID OUTC COD
121431553 12143155 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121431553 12143155 Bone erosion
121431553 12143155 Fistula
121431553 12143155 Gingivitis
121431553 12143155 Inflammation
121431553 12143155 Oral pustule
121431553 12143155 Osteonecrosis of jaw
121431553 12143155 Periodontal disease
121431553 12143155 Tooth loss

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
121431553 12143155 1 2012 0
121431553 12143155 2 2013 0
121431553 12143155 3 2014 0
121431553 12143155 4 20151111 0