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
127464521 12746452 1 I 201607 20160708 20160915 20160915 EXP BR-EMD SERONO-8096219 EMD SERONO INC 56.29 YR M Y 55.00000 KG 20160915 CN BR BR

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
127464521 12746452 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous INITIAL TITRATION DOSE (UNSPECIFIED) AU014543 103780 INJECTION TIW
127464521 12746452 2 SS REBIF INTERFERON BETA-1A 1 Subcutaneous FULL DOSE OF REBIF (0.5 ML) AU014543 103780 44 UG INJECTION TIW
127464521 12746452 3 SS REBIF INTERFERON BETA-1A 1 Subcutaneous AU014543 103780 22 UG INJECTION TIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127464521 12746452 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
127464521 12746452 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127464521 12746452 Asthenia
127464521 12746452 Gait disturbance
127464521 12746452 Multiple sclerosis relapse
127464521 12746452 Paralysis
127464521 12746452 Sensory loss
127464521 12746452 Thirst

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
127464521 12746452 1 20160704 0
127464521 12746452 2 20160708 0