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
127885751 12788575 1 I 20160113 20160928 20160928 EXP PHHY2016BR004928 NOVARTIS 0.00 F Y 41.00000 KG 20160928 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
127885751 12788575 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO D 21817 5 MG SOLUTION FOR INJECTION
127885751 12788575 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO D 21817 5 MG SOLUTION FOR INJECTION
127885751 12788575 3 C OSTEOPAN 2 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127885751 12788575 1 Osteoporosis
127885751 12788575 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127885751 12788575 DS
127885751 12788575 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127885751 12788575 Fall
127885751 12788575 Limb injury
127885751 12788575 Pain in extremity
127885751 12788575 Peripheral swelling
127885751 12788575 Upper limb fracture
127885751 12788575 Wrist fracture

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
127885751 12788575 1 20141204 0
127885751 12788575 2 20151127 0