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
120542814 12054281 4 F 20141025 20160822 20160209 20160826 PER PHHY2016US012819 NOVARTIS 34.77 YR F Y 0.00000 20160826 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
120542814 12054281 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral UNK 22527 CAPSULE
120542814 12054281 2 SS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral UNK 22527 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120542814 12054281 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
120542814 12054281 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120542814 12054281 Alopecia
120542814 12054281 Arthralgia
120542814 12054281 Balance disorder
120542814 12054281 Depression
120542814 12054281 Haematocrit decreased
120542814 12054281 Haemoglobin decreased
120542814 12054281 Headache
120542814 12054281 Hypoaesthesia
120542814 12054281 Memory impairment
120542814 12054281 Pain
120542814 12054281 Seizure
120542814 12054281 Sensory disturbance
120542814 12054281 Sinusitis
120542814 12054281 Urinary tract infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found