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
127069041 12706904 1 I 20160718 20160901 20160901 PER US-TEVA-678841USA TEVA 0.00 F Y 77.18000 KG 20160901 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
127069041 12706904 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous 20622 INJECTION
127069041 12706904 2 SS AMPYRA DALFAMPRIDINE 1 Oral 20 MILLIGRAM DAILY; TNKN 0 10 MG TABLET BID
127069041 12706904 3 SS AMPYRA DALFAMPRIDINE 1 Oral 20 MILLIGRAM DAILY; TNKN 0 10 MG TABLET BID
127069041 12706904 4 C MULTIVITAMIN VITAMINS 1 0
127069041 12706904 5 C VITAMIN D CHOLECALCIFEROL 1 0
127069041 12706904 6 C LORATADINE. LORATADINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127069041 12706904 1 Multiple sclerosis
127069041 12706904 2 Gait disturbance

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127069041 12706904 Injection site pruritus
127069041 12706904 Insomnia
127069041 12706904 Pruritus

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
127069041 12706904 2 2011 0
127069041 12706904 3 2015 0