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
126429271 12642927 1 I 20160802 20160803 20160811 20160811 EXP CA-TEVA-683678ACC TEVA 21.12 YR M Y 0.00000 20160811 CN CA CA

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
126429271 12642927 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous 20 MILLIGRAM DAILY; 20622 20 MG INJECTION QD
126429271 12642927 2 C VITAMIN D CHOLECALCIFEROL 1 0
126429271 12642927 3 C Omega 3 Complex 2 0
126429271 12642927 4 C Omega B Complex 2 0
126429271 12642927 5 C Vitamin B VITAMIN B 1 0
126429271 12642927 6 C VITAMIN B12 CYANOCOBALAMIN 1 0
126429271 12642927 7 C Probiotic PROBIOTICS NOS 1 0
126429271 12642927 8 C FOLIC ACID. FOLIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126429271 12642927 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
126429271 12642927 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126429271 12642927 Dyspnoea
126429271 12642927 Loss of consciousness

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
126429271 12642927 1 20160610 0