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
127252521 12725252 1 I 20160825 0 20160906 20160906 DIR FDA-CTU 61.00 YR F N 0.00000 20160906 N 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
127252521 12725252 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous D D AU016901 20180228 0 44 UG TIW
127252521 12725252 2 C TEGRETOL CARBAMAZEPINE 1 0
127252521 12725252 3 C VITAMIN E .ALPHA.-TOCOPHEROL 1 0
127252521 12725252 4 C VITAMIN D CHOLECALCIFEROL 1 0
127252521 12725252 5 C VITAMIN B VITAMIN B 1 0
127252521 12725252 6 C DIAZEPAM. DIAZEPAM 1 0
127252521 12725252 7 C BACLOFEN. BACLOFEN 1 0
127252521 12725252 8 C DIOVAN VALSARTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127252521 12725252 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127252521 12725252 Cataract operation
127252521 12725252 Multiple sclerosis relapse

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

Event ID CASEID RPSR COD
127252521 12725252 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127252521 12725252 1 20140625 0