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
122903162 12290316 2 F 20160812 20160421 20160818 EXP PHEH2016US009775 NOVARTIS 0.00 M Y 0.00000 20160818 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
122903162 12290316 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.0625 MG (0.25 ML), QOD (WEEKS 1-2) 125290 .062 MG SOLUTION FOR INJECTION
122903162 12290316 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.125 MG (0.5 ML), QOD (WEEKS 3-4) 125290 .125 MG SOLUTION FOR INJECTION
122903162 12290316 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.1875 MG (0.75 ML), QOD (WEEKS 5-6) 125290 .185 MG SOLUTION FOR INJECTION
122903162 12290316 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous 0.25 MG (1 ML), QOD (WEEKS 7+) 125290 .25 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122903162 12290316 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
122903162 12290316 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122903162 12290316 Central nervous system lesion
122903162 12290316 Drug ineffective
122903162 12290316 Insomnia

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

no results found

Therapies reported

no results found