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
124821622 12482162 2 F 2015 20160712 20160620 20160718 EXP PHHY2016BR083556 NOVARTIS 0.00 F Y 54.00000 KG 20160718 MD BR BR

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
124821622 12482162 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
124821622 12482162 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124821622 12482162 1 Osteoporosis
124821622 12482162 2 Mineral supplementation

Outcome of event

Event ID CASEID OUTC COD
124821622 12482162 LT
124821622 12482162 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124821622 12482162 Asthenia
124821622 12482162 Blood pressure increased
124821622 12482162 Dizziness
124821622 12482162 Drug intolerance
124821622 12482162 Fall
124821622 12482162 Feeling abnormal
124821622 12482162 Gait disturbance
124821622 12482162 Hernia
124821622 12482162 Malaise
124821622 12482162 Middle insomnia

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
124821622 12482162 1 20150323 0
124821622 12482162 2 201606 0