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
94316332 9431633 2 F 20120701 20130808 20130731 20130816 EXP US-BIOGENIDEC-2013BI069347 BIOGEN 65.65 YR F Y 0.00000 20130816 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
94316332 9431633 1 PS AVONEX 1 INTRAMUSCULAR D 103628 30 UG /wk
94316332 9431633 2 SS AVONEX 1 INTRAMUSCULAR D 103628 30 UG /wk
94316332 9431633 3 SS AVONEX 1 INTRAMUSCULAR D 103628 30 UG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94316332 9431633 1 Multiple sclerosis
94316332 9431633 2 Multiple sclerosis
94316332 9431633 3 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
94316332 9431633 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
94316332 9431633 Anxiety
94316332 9431633 Arthralgia
94316332 9431633 Blister
94316332 9431633 Feeling cold
94316332 9431633 Gastrooesophageal reflux disease
94316332 9431633 Irritable bowel syndrome
94316332 9431633 Multiple sclerosis relapse
94316332 9431633 Peripheral nerve injury

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
94316332 9431633 1 20050502 20050801 0
94316332 9431633 2 20111201 20120508 0
94316332 9431633 3 20120701 0