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
120095413 12009541 3 F 2015 20160620 20160205 20160701 EXP AU-EMD SERONO-8065917 EMD SERONO INC 0.00 F Y 0.00000 20160701 CN AU AU

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
120095413 12009541 1 PS REBIF INTERFERON BETA-1A 1 N 103780
120095413 12009541 2 SS REBIF INTERFERON BETA-1A 1 TITRATED TO FULL DOSE (UNSPECIFIED) N 103780
120095413 12009541 3 C VITAMIN D /00107901/ ERGOCALCIFEROL 1 0
120095413 12009541 4 C MICROLUT 2 RECOMMENCED AT AN UNKNOWN DOSAGE 0
120095413 12009541 5 C VITAMIN B2 /00154901/ 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120095413 12009541 1 Multiple sclerosis
120095413 12009541 3 Product used for unknown indication
120095413 12009541 4 Product used for unknown indication
120095413 12009541 5 Vitamin supplementation

Outcome of event

Event ID CASEID OUTC COD
120095413 12009541 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120095413 12009541 Fatigue
120095413 12009541 Headache
120095413 12009541 Migraine

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
120095413 12009541 1 201505 0
120095413 12009541 2 201507 20160205 0