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
125453551 12545355 1 I 20160629 20160711 20160711 EXP US-BAYER-2016-128875 BAYER 0.00 F Y 88.40000 KG 20160711 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
125453551 12545355 1 PS BETASERON INTERFERON BETA-1B 1 103471 POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
125453551 12545355 2 C AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 0 10 MG BID
125453551 12545355 3 C GILENYA FINGOLIMOD HYDROCHLORIDE 1 Unknown UNK 0
125453551 12545355 4 C COPAXONE GLATIRAMER ACETATE 1 0
125453551 12545355 5 C REBIF INTERFERON BETA-1A 1 0
125453551 12545355 6 C BACLOFEN. BACLOFEN 1 UNK 0
125453551 12545355 7 C PROVIGIL MODAFINIL 1 UNK 0
125453551 12545355 8 C VOLTAREN DICLOFENAC SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125453551 12545355 1 Multiple sclerosis
125453551 12545355 2 Gait disturbance
125453551 12545355 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125453551 12545355 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125453551 12545355 Back pain
125453551 12545355 Drug ineffective
125453551 12545355 Full blood count decreased
125453551 12545355 Gait disturbance
125453551 12545355 Secondary progressive multiple sclerosis

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
125453551 12545355 2 20141118 201507 0
125453551 12545355 3 201106 20150915 0