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
126390091 12639009 1 I 2009 20130403 20160809 20160809 EXP BR-EMD SERONO-7203354 EMD SERONO INC 35.76 YR F Y 0.00000 20160810 CN BR BR

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
126390091 12639009 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous AU003207,AU012339 103780 44 UG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126390091 12639009 1 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
126390091 12639009 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126390091 12639009 Dengue fever
126390091 12639009 Drug dose omission
126390091 12639009 Headache
126390091 12639009 Inappropriate schedule of drug administration
126390091 12639009 Injection site erythema
126390091 12639009 Neck pain
126390091 12639009 Pain
126390091 12639009 Sensory disturbance
126390091 12639009 Tension
126390091 12639009 Vision blurred

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
126390091 12639009 1 20090128 0