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
126300641 12630064 1 I 20160707 20160711 20160808 20160808 PER US-BAYER-2016-136178 BAYER 62.00 YR A F Y 0.00000 20160808 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
126300641 12630064 1 PS BETASERON INTERFERON BETA-1B 1 Subcutaneous 8 MIU, QOD 52197A 103471 8 MIU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
126300641 12630064 2 SS BETASERON INTERFERON BETA-1B 1 Subcutaneous 0.3 MG, QOD 103471 .3 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126300641 12630064 1 Relapsing-remitting multiple sclerosis
126300641 12630064 2 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
126300641 12630064 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126300641 12630064 Arthralgia
126300641 12630064 Chills
126300641 12630064 Erythema
126300641 12630064 Feeling hot
126300641 12630064 Musculoskeletal pain
126300641 12630064 Pain in extremity
126300641 12630064 Skin mass

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
126300641 12630064 1 19990427 0
126300641 12630064 2 20130116 0