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
121732444 12173244 4 F 201601 20160829 20160311 20160906 EXP US-BIOGEN-2016BI00196444 BIOGEN 63.52 YR F Y 0.00000 20160906 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
121732444 12173244 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG POWDER FOR SOLUTION FOR INJECTION /wk
121732444 12173244 2 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN
121732444 12173244 3 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN
121732444 12173244 4 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121732444 12173244 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
121732444 12173244 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121732444 12173244 Adverse drug reaction
121732444 12173244 Bone pain
121732444 12173244 Breast cancer
121732444 12173244 Malaise
121732444 12173244 Multiple sclerosis relapse
121732444 12173244 Musculoskeletal stiffness
121732444 12173244 Myalgia
121732444 12173244 Pain

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
121732444 12173244 1 200402 0
121732444 12173244 2 20110516 20160302 0
121732444 12173244 3 20021029 0
121732444 12173244 4 19981101 0