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
123388112 12338811 2 F 20160708 20160505 20160713 PER PHEH2016US011079 NOVARTIS 0.00 M Y 0.00000 20160713 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
123388112 12338811 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.0625 MG (0.25 ML) FOR WEEK 1 TO 2, QOD Y 125290 .062 MG SOLUTION FOR INJECTION
123388112 12338811 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.125 MG (0.5 ML) FOR WEEK 3 TO 4, QOD Y 125290 .125 MG SOLUTION FOR INJECTION
123388112 12338811 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.1875 MG (0.75 ML) FOR WEEK 5 TO 6, QOD Y 125290 .187 MG SOLUTION FOR INJECTION
123388112 12338811 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.25 MG (1 ML) FOR WEEK 7+, QOD Y 125290 .25 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123388112 12338811 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123388112 12338811 Influenza like illness
123388112 12338811 Injection site bruising

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
123388112 12338811 1 20160427 0