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
120694603 12069460 3 F 201601 20160805 20160211 20160824 PER US-BAYER-2016-027494 BAYER 40.00 YR A F Y 0.00000 20160825 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
120694603 12069460 1 PS BETASERON INTERFERON BETA-1B 1 Subcutaneous 0.125 MG, QOD 52417A 103471 .125 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
120694603 12069460 2 SS BETASERON INTERFERON BETA-1B 1 Subcutaneous 0.25 MG, UNK 103471 .25 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120694603 12069460 1 Multiple sclerosis
120694603 12069460 2 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120694603 12069460 Contusion
120694603 12069460 Decreased interest
120694603 12069460 Depressed mood
120694603 12069460 Drug ineffective
120694603 12069460 Hypoaesthesia
120694603 12069460 Injection site mass
120694603 12069460 Myalgia
120694603 12069460 Paraesthesia
120694603 12069460 Sinusitis

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
120694603 12069460 1 20160116 0
120694603 12069460 2 201603 0