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
127725551 12772555 1 I 20160920 20160922 20160922 PER PHEH2016US024249 NOVARTIS 0.00 F Y 0.00000 20160922 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
127725551 12772555 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.062 MG, QOD(0.25ML) 61264_A 125290 .062 MG SOLUTION FOR INJECTION
127725551 12772555 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.125 MG, QOD(0.5ML) 61264_A 125290 .125 MG SOLUTION FOR INJECTION
127725551 12772555 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.187 MG, QOD(0.75ML) 61264_A 125290 .187 MG SOLUTION FOR INJECTION
127725551 12772555 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.25 UNK, UNK(1 ML) 61264_A 125290 .25 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127725551 12772555 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127725551 12772555 Abdominal pain upper
127725551 12772555 Diarrhoea
127725551 12772555 Oropharyngeal pain

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
127725551 12772555 1 20160913 0