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
124488383 12448838 3 F 20160620 20160811 20160608 20160816 EXP PHHY2016BR062126 NOVARTIS 77.02 YR F Y 83.00000 KG 20160816 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
124488383 12448838 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
124488383 12448838 2 C SELOZOK METOPROLOL SUCCINATE 1 Unknown U 0
124488383 12448838 3 C ENBREL ETANERCEPT 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124488383 12448838 1 Osteoporosis
124488383 12448838 2 Product used for unknown indication
124488383 12448838 3 Rheumatic disorder

Outcome of event

Event ID CASEID OUTC COD
124488383 12448838 HO
124488383 12448838 LT
124488383 12448838 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124488383 12448838 Abasia
124488383 12448838 Erysipelas
124488383 12448838 Hypersensitivity
124488383 12448838 Ligament sprain
124488383 12448838 Peripheral swelling
124488383 12448838 Pruritus generalised
124488383 12448838 Pyrexia
124488383 12448838 Rash
124488383 12448838 Thrombophlebitis
124488383 12448838 Thrombosis

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
124488383 12448838 1 20150430 20150430 0