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
126444751 12644475 1 I 20160808 20160811 20160811 PER PHEH2016US019939 NOVARTIS 0.00 F Y 0.00000 20160811 CN COUNTRY NOT SPECIFIED 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
126444751 12644475 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.062 MG (0.25 ML), QOD WEEKS 1-2 U 125290 .062 MG
126444751 12644475 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.125 MG (0.5ML), QOD WEEKS 3-4 U 125290 .125 MG
126444751 12644475 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.187MG (0.75ML), QOD WEEKS 5-6 U 125290 .187 MG
126444751 12644475 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.25MG (1 ML), QOD WEEK 7+ U 125290 .25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126444751 12644475 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126444751 12644475 Injection site erythema
126444751 12644475 Injection site pain
126444751 12644475 Injection site reaction

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found