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
125500112 12550011 2 F 20160628 20160914 20160712 20160922 EXP GB-BIOGEN-2016BI00263833 BIOGEN 34.53 YR F Y 0.00000 20160922 MD GB GB

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
125500112 12550011 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
125500112 12550011 2 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown 0 50 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125500112 12550011 1 Multiple sclerosis
125500112 12550011 2 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125500112 12550011 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125500112 12550011 Drug dose omission
125500112 12550011 Haemangioma
125500112 12550011 Malaise
125500112 12550011 Migraine
125500112 12550011 Seizure

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
125500112 12550011 1 20110921 0