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
126205662 12620566 2 F 20160826 20160804 20160830 PER PHEH2016US019407 NOVARTIS 0.00 F Y 0.00000 20160830 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
126205662 12620566 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.25 ML (0.0625 MG), QOD (WEEK 1-2) 125290 .25 ML SOLUTION FOR INJECTION
126205662 12620566 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.5 ML (0.125 MG), QOD (WEEK 3-4) 125290 .5 ML SOLUTION FOR INJECTION
126205662 12620566 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.75 ML (0.1875 MG), QOD (WEEK 5-6) 125290 .75 ML SOLUTION FOR INJECTION
126205662 12620566 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 1 ML (0.25 MG), QOD (WEEK 7 PLUS) 125290 1 ML SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126205662 12620566 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126205662 12620566 Malaise
126205662 12620566 Nasal congestion
126205662 12620566 Nasopharyngitis
126205662 12620566 Oropharyngeal pain
126205662 12620566 Rhinorrhoea

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
126205662 12620566 1 20160727 0
126205662 12620566 4 20160802 0