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
122023526 12202352 6 F 20160704 20160322 20160711 EXP PHHY2016BR037190 NOVARTIS 0.00 F Y 76.00000 KG 20160711 OT 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
122023526 12202352 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, Q12MO 21817 1 DF SOLUTION FOR INJECTION
122023526 12202352 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, Q12MO SC542 21817 1 DF SOLUTION FOR INJECTION
122023526 12202352 3 C CALCIUM CALCIUM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122023526 12202352 1 Osteoporosis
122023526 12202352 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122023526 12202352 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122023526 12202352 Arthralgia
122023526 12202352 Fall
122023526 12202352 Inappropriate schedule of drug administration
122023526 12202352 Influenza
122023526 12202352 Intervertebral disc protrusion
122023526 12202352 Lower limb fracture
122023526 12202352 Malaise
122023526 12202352 Pain
122023526 12202352 Patient-device incompatibility
122023526 12202352 Spinal pain
122023526 12202352 Urinary tract infection
122023526 12202352 Visual impairment

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
122023526 12202352 1 20150520 0
122023526 12202352 2 20160329 0