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
124331752 12433175 2 F 201605 20160628 20160603 20160708 EXP US-BAYER-2016-103929 BAYER 49.00 YR A F Y 0.00000 20160708 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
124331752 12433175 1 PS BETASERON INTERFERON BETA-1B 1 Subcutaneous 2 MIU, QOD 103471 2 MIU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
124331752 12433175 2 SS BETASERON INTERFERON BETA-1B 1 Subcutaneous 8 MIU, QOD 103471 8 MIU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION QOD
124331752 12433175 3 C ALEVE NAPROXEN SODIUM 1 0 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124331752 12433175 1 Multiple sclerosis
124331752 12433175 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
124331752 12433175 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124331752 12433175 Fatigue
124331752 12433175 Gait disturbance
124331752 12433175 Nausea
124331752 12433175 Pain
124331752 12433175 Vomiting

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
124331752 12433175 1 20160511 2016 0
124331752 12433175 2 2016 0