The Safety Rates Drug Report

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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
122616112 12261611 2 F 2016 20160726 20160412 20160913 PER US-TEVA-647134USA TEVA 0.00 F Y 0.00000 20160913 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
122616112 12261611 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous V01881 20622 40 MG INJECTION TIW
122616112 12261611 2 C BACLOFEN. BACLOFEN 1 Unknown 0
122616112 12261611 3 C CRYSELLE ETHINYL ESTRADIOLNORGESTREL 1 Unknown 0
122616112 12261611 4 C ESCITALOPRAM ESCITALOPRAM OXALATE 1 Unknown 0
122616112 12261611 5 C VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Unknown 0
122616112 12261611 6 C LOW-OGESTREL ETHINYL ESTRADIOLNORGESTREL 1 Unknown 0
122616112 12261611 7 C VITAMIN D CHOLECALCIFEROL 1 Unknown 0 50000 IU
122616112 12261611 8 C DULOXETINE. DULOXETINE 1 Unknown 0
122616112 12261611 9 C OXYBUTYNIN OXYBUTYNIN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122616112 12261611 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122616112 12261611 Drug dose omission
122616112 12261611 Hypoaesthesia oral

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
122616112 12261611 1 20150721 0