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
106988783 10698878 3 F 201406 20160729 20150108 20160811 EXP FR-EMD SERONO-8004189 EMD SERONO INC 25.62 YR F Y 0.00000 20160811 CN FR FR

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
106988783 10698878 1 PS REBIF INTERFERON BETA-1A 1 103780 44 UG INJECTION TIW
106988783 10698878 2 SS REBIF INTERFERON BETA-1A 1 103780 44 UG TIW
106988783 10698878 3 C UVEDOSE CHOLECALCIFEROL 1 Oral 0 1 DF /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106988783 10698878 1 Multiple sclerosis
106988783 10698878 3 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
106988783 10698878 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106988783 10698878 Abortion spontaneous
106988783 10698878 Injection site erythema
106988783 10698878 Injection site inflammation
106988783 10698878 Injection site pain
106988783 10698878 Maternal exposure during pregnancy

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
106988783 10698878 1 20140630 201410 0
106988783 10698878 2 201412 0
106988783 10698878 3 2014 0