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
125725171 12572517 1 I 20160219 20160719 20160719 EXP BR-BIOGEN-2016BI00194189 BIOGEN 0.00 F Y 0.00000 20160719 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
125725171 12572517 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
125725171 12572517 2 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Unknown 0 150 MG UNKNOWN QD
125725171 12572517 3 C DIANE (CYPROTERONE ACETATEETHINYL ESTRADIOL) CYPROTERONE ACETATEETHINYL ESTRADIOL 1 Unknown 0 35 MG UNKNOWN
125725171 12572517 4 C RIVOTRIL CLONAZEPAM 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125725171 12572517 1 Multiple sclerosis
125725171 12572517 2 Depression
125725171 12572517 3 Contraception
125725171 12572517 4 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
125725171 12572517 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125725171 12572517 Arthralgia
125725171 12572517 Burning sensation
125725171 12572517 Chills
125725171 12572517 Headache
125725171 12572517 Multiple sclerosis
125725171 12572517 Nausea
125725171 12572517 Pain
125725171 12572517 Pyrexia
125725171 12572517 Rash erythematous
125725171 12572517 Syncope
125725171 12572517 Vomiting
125725171 12572517 Weight abnormal

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
125725171 12572517 1 201511 201512 0