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
111716003 11171600 3 F 2015 20160713 20150608 20160721 EXP US-SA-2014SA084581 AVENTIS 58.00 YR A M Y 0.00000 20160721 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
111716003 11171600 1 PS AUBAGIO TERIFLUNOMIDE 1 Oral UNKNOWN 202992 14 MG QD
111716003 11171600 2 SS AMPYRA DALFAMPRIDINE 1 Oral UNK 0 10 MG TABLET BID
111716003 11171600 3 SS TYSABRI NATALIZUMAB 1 Unknown U UNK 0
111716003 11171600 4 C TOPROL XL METOPROLOL SUCCINATE 1 0
111716003 11171600 5 C CELEXA CITALOPRAM HYDROBROMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111716003 11171600 1 Multiple sclerosis
111716003 11171600 2 Gait disturbance

Outcome of event

Event ID CASEID OUTC COD
111716003 11171600 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111716003 11171600 Balance disorder
111716003 11171600 Condition aggravated
111716003 11171600 Confusional state
111716003 11171600 Drug dose omission
111716003 11171600 Fatigue
111716003 11171600 Head discomfort
111716003 11171600 Hepatitis C
111716003 11171600 Hypoaesthesia
111716003 11171600 Inappropriate schedule of drug administration
111716003 11171600 Infection susceptibility increased
111716003 11171600 JC virus test positive
111716003 11171600 Memory impairment
111716003 11171600 Mental impairment
111716003 11171600 Micturition urgency
111716003 11171600 Muscle spasms
111716003 11171600 Muscular weakness
111716003 11171600 Temperature intolerance
111716003 11171600 Visual acuity reduced

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
111716003 11171600 1 20140523 0
111716003 11171600 2 20110214 0