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
123525883 12352588 3 F 20160321 20160705 20160510 20160714 EXP US-BAYER-2016-085804 BAYER 54.00 YR A F Y 0.00000 20160714 OT 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
123525883 12352588 1 PS BETASERON INTERFERON BETA-1B 1 Subcutaneous 6 MIU, QOD 103471 6 MIU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
123525883 12352588 2 SS BETASERON INTERFERON BETA-1B 1 Subcutaneous 2 MIU, QOD 103471 2 MIU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
123525883 12352588 3 SS BETACONNECT DEVICE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123525883 12352588 1 Multiple sclerosis
123525883 12352588 2 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
123525883 12352588 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123525883 12352588 Dysstasia
123525883 12352588 Fall
123525883 12352588 Fatigue
123525883 12352588 Gait disturbance
123525883 12352588 Injection site bruising
123525883 12352588 Injection site erythema
123525883 12352588 Muscular weakness

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
123525883 12352588 1 20160321 0
123525883 12352588 2 20160321 20160508 0
123525883 12352588 3 20160321 0