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
119092313 11909231 3 F 201509 20160715 20160112 20160720 PER PHEH2016US000881 NOVARTIS 19.67 YR F Y 57.60000 KG 20160720 OT US US

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
119092313 11909231 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.25 ML (0.0625 MG) (WEEKS 1-2), QOD 125290 .25 ML SOLUTION FOR INJECTION
119092313 11909231 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.5 ML (0.125 MG) (WEEKS 3-4), QOD 125290 .5 ML SOLUTION FOR INJECTION
119092313 11909231 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.75 ML (0.1875 MG) (WEEKS 5-6), QOD 125290 .75 ML SOLUTION FOR INJECTION
119092313 11909231 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 1 ML (0.25 MG) (WEEKS 7+), QOD 125290 1 ML SOLUTION FOR INJECTION
119092313 11909231 5 C VITAMIN D CHOLECALCIFEROL 1 Oral UNK UNK, QD 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119092313 11909231 1 Multiple sclerosis
119092313 11909231 5 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119092313 11909231 Injection site bruising
119092313 11909231 Injection site pain
119092313 11909231 Pain
119092313 11909231 Pain in extremity

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
119092313 11909231 1 201509 0