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
121966803 12196680 3 F 20150911 20160809 20160321 20160815 EXP CO-BIOGEN-2015BI129805 BIOGEN 0.00 A F Y 64.00000 KG 20160815 CN CO CO

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
121966803 12196680 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 150886A 103628 UNKNOWN /wk
121966803 12196680 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular 150886A 103628 UNKNOWN /wk
121966803 12196680 3 C LYRICA PREGABALIN 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121966803 12196680 1 Product used for unknown indication
121966803 12196680 3 Pain

Outcome of event

Event ID CASEID OUTC COD
121966803 12196680 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121966803 12196680 Arthralgia
121966803 12196680 Chills
121966803 12196680 Depression
121966803 12196680 Headache
121966803 12196680 Malaise
121966803 12196680 Mobility decreased
121966803 12196680 Neuromyelitis optica spectrum disorder
121966803 12196680 Odynophagia
121966803 12196680 Oral disorder
121966803 12196680 Pyrexia
121966803 12196680 Sensation of foreign body
121966803 12196680 Sensory loss

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
121966803 12196680 1 20160412 0