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
127763451 12776345 1 I 20160920 20160923 20160923 PER PHEH2016US024411 NOVARTIS 0.00 F Y 0.00000 20160923 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
127763451 12776345 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 1-2: 0.0625 MG (0.25 ML),QOD 61264-A 125290 .062 MG SOLUTION FOR INJECTION
127763451 12776345 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 3-4: 0.125 MG (0.5 ML),QOD 61264-A 125290 .125 MG SOLUTION FOR INJECTION
127763451 12776345 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 5-6: 0.1875 MG (0.75 ML),QOD 61264-A 125290 .187 MG SOLUTION FOR INJECTION
127763451 12776345 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 7 PLUS: 0.25 MG (1 ML), QOD 61264-A 125290 .25 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127763451 12776345 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127763451 12776345 Injection site pruritus
127763451 12776345 Injection site swelling

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

no results found

Therapies reported

no results found