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
124887936 12488793 6 F 20160525 20160812 20160622 20160822 EXP PHHY2016KR075062 NOVARTIS 60.00 YR F Y 52.00000 KG 20160822 CN KR KR

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
124887936 12488793 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, ONCE/SINGLE 0 5 MG SOLUTION FOR INJECTION 1X

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124887936 12488793 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
124887936 12488793 HO
124887936 12488793 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124887936 12488793 Abnormal sensation in eye
124887936 12488793 Blister
124887936 12488793 Burning sensation
124887936 12488793 Chills
124887936 12488793 Cough
124887936 12488793 Dysuria
124887936 12488793 Erythema
124887936 12488793 Eye pain
124887936 12488793 Flushing
124887936 12488793 Headache
124887936 12488793 Peripheral swelling
124887936 12488793 Pollakiuria
124887936 12488793 Poor quality sleep
124887936 12488793 Pyrexia
124887936 12488793 Rhinalgia
124887936 12488793 Tunnel vision

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
124887936 12488793 1 20160524 0