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
126064031 12606403 1 I 20160721 0 20160728 20160728 DIR 53.00 YR F N 0.00000 20160727 N PH 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
126064031 12606403 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous 44MCG 3X/WEEK SC D D AU015917 20170930 0 44 UG TIW
126064031 12606403 3 C ASPIRIN. ASPIRIN 1 0
126064031 12606403 5 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 0
126064031 12606403 7 C GABAPENTIN. GABAPENTIN 1 0
126064031 12606403 9 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0
126064031 12606403 11 C CELEXA CITALOPRAM HYDROBROMIDE 1 0
126064031 12606403 13 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
126064031 12606403 15 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 0
126064031 12606403 17 C VITAMIN D2 ERGOCALCIFEROL 1 0
126064031 12606403 19 C BACLOFEN. BACLOFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126064031 12606403 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
126064031 12606403 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126064031 12606403 Disease recurrence
126064031 12606403 Influenza like illness

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

Event ID CASEID RPSR COD
126064031 12606403 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126064031 12606403 1 20160304 0