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
127263432 12726343 2 F 2016 20160907 20160908 20160915 EXP US-BAYER-2016-170788 BAYER 61.00 YR A F Y 0.00000 20160915 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
127263432 12726343 1 PS BETASERON INTERFERON BETA-1B 1 Subcutaneous 0.3 MG, QOD 52199A 103471 .3 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
127263432 12726343 2 SS BETASERON INTERFERON BETA-1B 1 Subcutaneous 0.3 MG, QOD 52199A 103471 .3 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127263432 12726343 1 Multiple sclerosis
127263432 12726343 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
127263432 12726343 OT
127263432 12726343 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127263432 12726343 Delusion
127263432 12726343 Depression
127263432 12726343 Hypoaesthesia
127263432 12726343 Multiple sclerosis relapse
127263432 12726343 Muscle spasms
127263432 12726343 Stress
127263432 12726343 Urticaria

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
127263432 12726343 1 2005 0
127263432 12726343 2 201007 0