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
112530833 11253083 3 F 20140507 20160725 20150709 20160728 PER PHHY2014US099457 NOVARTIS 64.57 YR F Y 0.00000 20160728 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
112530833 11253083 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 22527 CAPSULE
112530833 11253083 2 C AMPYRA DALFAMPRIDINE 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112530833 11253083 1 Multiple sclerosis
112530833 11253083 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
112530833 11253083 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112530833 11253083 Alanine aminotransferase increased
112530833 11253083 Aspartate aminotransferase increased
112530833 11253083 Blood alkaline phosphatase increased
112530833 11253083 Blood creatinine increased
112530833 11253083 Low density lipoprotein increased
112530833 11253083 Lymphocyte count decreased
112530833 11253083 Lymphocyte count increased
112530833 11253083 Monocyte count increased
112530833 11253083 White blood cell count decreased

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
112530833 11253083 2 20140507 20150105 0