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
126960511 12696051 1 I 20121116 20121116 20160829 20160829 EXP US-EMD SERONO-7176976 EMD SERONO INC 30.88 YR F Y 0.00000 20160830 MD US US

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
126960511 12696051 1 PS REBIF INTERFERON BETA-1A 1 Subcutaneous Y 103780 44 UG INJECTION TIW
126960511 12696051 2 SS AMANTADINE AMANTADINE 1 Y 0 100 MG TID
126960511 12696051 3 C FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 0
126960511 12696051 4 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 0 30 MG QD
126960511 12696051 5 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0 150 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126960511 12696051 1 Multiple sclerosis
126960511 12696051 2 Fatigue
126960511 12696051 3 Hypersensitivity
126960511 12696051 4 Attention deficit/hyperactivity disorder
126960511 12696051 5 Feeling of relaxation

Outcome of event

Event ID CASEID OUTC COD
126960511 12696051 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126960511 12696051 Balance disorder
126960511 12696051 Fatigue
126960511 12696051 Multiple sclerosis relapse
126960511 12696051 Schizophrenia
126960511 12696051 Vision blurred

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
126960511 12696051 1 20120509 20121121 0
126960511 12696051 2 20121114 20121121 0