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
125251931 12525193 1 I 201606 20160627 20160704 20160704 PER US-TEVA-673408USA TEVA 66.57 YR F Y 0.00000 20160704 PH 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
125251931 12525193 1 PS COPAXONE GLATIRAMER ACETATE 1 Subcutaneous V02001 20622 40 MG INJECTION TIW
125251931 12525193 2 C DILTIAZEM. DILTIAZEM 1 Unknown 0
125251931 12525193 3 C PREDNISOLONE. PREDNISOLONE 1 Unknown 0
125251931 12525193 4 C TOPAMAX TOPIRAMATE 1 Unknown 0
125251931 12525193 5 C LYRICA PREGABALIN 1 Unknown 0
125251931 12525193 6 C ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 Unknown 0
125251931 12525193 7 C KEFLEX CEPHALEXIN 1 Unknown 0
125251931 12525193 8 C STRATTERA ATOMOXETINE HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125251931 12525193 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125251931 12525193 Fatigue

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

no results found

Therapies reported

no results found