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
126646471 12664647 1 I 20141205 20160818 20160818 EXP PHHY2014BR162421 NOVARTIS 0.00 F Y 46.00000 KG 20160818 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
126646471 12664647 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
126646471 12664647 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
126646471 12664647 3 C CALCIUM CALCIUM 1 Unknown 2 DF, QD 0 2 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126646471 12664647 1 Osteoporosis
126646471 12664647 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126646471 12664647 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126646471 12664647 Abasia
126646471 12664647 Arthralgia
126646471 12664647 Asthenia
126646471 12664647 Balance disorder
126646471 12664647 Fibromyalgia
126646471 12664647 Finger deformity
126646471 12664647 Malaise
126646471 12664647 Muscular weakness
126646471 12664647 Nervousness
126646471 12664647 Neuritis
126646471 12664647 Pain
126646471 12664647 Pain in extremity
126646471 12664647 Weight decreased

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
126646471 12664647 1 2011 0
126646471 12664647 2 2012 0
126646471 12664647 3 2011 0