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
120716985 12071698 5 F 20160209 20160916 20160212 20160921 EXP PHEH2016US003224 NOVARTIS 59.97 YR F Y 90.70000 KG 20160921 CN COUNTRY NOT SPECIFIED 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
120716985 12071698 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD U S0115 22527 .5 MG CAPSULE QD
120716985 12071698 2 SS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120716985 12071698 1 Multiple sclerosis
120716985 12071698 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120716985 12071698 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120716985 12071698 Blood pressure decreased
120716985 12071698 Decreased immune responsiveness
120716985 12071698 Fatigue
120716985 12071698 Feeling abnormal
120716985 12071698 Malaise
120716985 12071698 Nasal congestion
120716985 12071698 Pain
120716985 12071698 Post procedural contusion
120716985 12071698 Post procedural swelling
120716985 12071698 Tooth fracture

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
120716985 12071698 1 20160209 0