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
75467025 7546702 5 F 2010 20130919 20100819 20130930 EXP US-BIOGENIDEC-2010BI027583 BIOGEN 73.00 YR F Y 0.00000 20130930 MD US 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
75467025 7546702 1 PS AVONEX 1 INTRAMUSCULAR D 103628 30 UG POWDER FOR SOLUTION FOR INJECTION /wk
75467025 7546702 2 SS AVONEX 1 INTRAMUSCULAR D 103628 30 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
75467025 7546702 1 Multiple sclerosis
75467025 7546702 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
75467025 7546702 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
75467025 7546702 Balance disorder
75467025 7546702 Cerebrovascular accident
75467025 7546702 Gait disturbance
75467025 7546702 Hypoaesthesia
75467025 7546702 Insomnia
75467025 7546702 Joint swelling
75467025 7546702 Meniscus injury
75467025 7546702 Muscular weakness
75467025 7546702 Musculoskeletal discomfort
75467025 7546702 Musculoskeletal disorder
75467025 7546702 Pneumonia
75467025 7546702 Stress

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
75467025 7546702 1 19970201 200308 0
75467025 7546702 2 200308 0