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
126585281 12658528 1 I 20160815 0 20160816 20160816 DIR 71.00 YR F N 0.00000 20160815 Y 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
126585281 12658528 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D TCNV 20180430 0 10 MG Q12H
126585281 12658528 3 C ATORVASTATIN ATORVASTATIN 1 0
126585281 12658528 5 C BACLOFEN. BACLOFEN 1 0
126585281 12658528 7 C CYANOCOBALAMIN. CYANOCOBALAMIN 1 0
126585281 12658528 9 C OXYBUTYNIN OXYBUTYNIN 1 0
126585281 12658528 11 C LEVOTHYROXINE. LEVOTHYROXINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126585281 12658528 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
126585281 12658528 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126585281 12658528 Pruritus
126585281 12658528 Urticaria

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

Event ID CASEID RPSR COD
126585281 12658528 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126585281 12658528 1 20160725 0