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
122509702 12250970 2 F 2016 20160726 20160409 20160826 PER US-TEVA-647124USA TEVA 0.00 F Y 0.00000 20160826 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
122509702 12250970 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous C42189 20622 40 MG INJECTION TIW
122509702 12250970 2 C Complex B50 2 Unknown 0
122509702 12250970 3 C VITAMIN D CHOLECALCIFEROL 1 Unknown 0
122509702 12250970 4 C GLUCOSAMINE GLUCOSAMINE 1 Unknown 0
122509702 12250970 5 C OMEGA 3 OMEGA-3 FATTY ACIDS 1 Unknown 0
122509702 12250970 6 C CALCIUM CALCIUM 1 Unknown 0
122509702 12250970 7 C NORVASC AMLODIPINE BESYLATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122509702 12250970 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122509702 12250970 Fatigue
122509702 12250970 Increased appetite
122509702 12250970 Weight increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found