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
70328102 7032810 2 F 200902 20121220 20090625 20121231 EXP US-BIOGENIDEC-2009BI019059 BIOGEN 62.00 YR F Y 0.00000 20121231 CN 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
70328102 7032810 1 PS AVONEX 1 INTRAMUSCULAR D 103628 30 UG Injection /wk
70328102 7032810 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
70328102 7032810 1 Multiple sclerosis
70328102 7032810 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
70328102 7032810 HO
70328102 7032810 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
70328102 7032810 Breast cancer stage II
70328102 7032810 Central nervous system lesion
70328102 7032810 Drug ineffective
70328102 7032810 Hypotension
70328102 7032810 Laryngeal disorder
70328102 7032810 Loss of control of legs
70328102 7032810 Mastectomy
70328102 7032810 Multiple sclerosis
70328102 7032810 Renal failure

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
70328102 7032810 1 19961020 0