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
125442672 12544267 2 F 201601 20160721 20160711 20160804 EXP US-EMD SERONO-8088904 EMD SERONO INC 58.30 YR M Y 0.00000 20160804 OT 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
125442672 12544267 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous U AU013980 103780 INJECTION
125442672 12544267 2 SS REBIF INTERFERON BETA-1A 1 Subcutaneous U AU013980 103780 44 UG INJECTION TIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125442672 12544267 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125442672 12544267 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125442672 12544267 Asthenia
125442672 12544267 Fall
125442672 12544267 Gait disturbance
125442672 12544267 Hepatic enzyme increased
125442672 12544267 Hypersensitivity
125442672 12544267 Lethargy
125442672 12544267 Pyrexia

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
125442672 12544267 1 2009 0
125442672 12544267 2 201511 201601 0