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
88716303 8871630 3 F 20120628 20120426 20130107 PER PHEH2012US002680 NOVARTIS 42.00 YR F N 0.00000 20121205 CN 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
88716303 8871630 1 PS GILENYA 1 ORAL S0010A 20130228 22527 0.5 MG QD
88716303 8871630 3 C CYMBALTA 1 0
88716303 8871630 4 C LOESTRIN (ETHINYLESTRADIOL, NORETHISTERONE ACETATE) 2 0
88716303 8871630 6 C SUMATRIPTAN (SUMATRIPTAN) 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88716303 8871630 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
88716303 8871630 Cough
88716303 8871630 Dyspnoea
88716303 8871630 Head discomfort
88716303 8871630 Heart rate decreased
88716303 8871630 Nasopharyngitis
88716303 8871630 Oropharyngeal pain
88716303 8871630 Rash
88716303 8871630 Rhinorrhoea

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

Event ID CASEID RPSR COD
88716303 8871630 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
88716303 8871630 1 20110921 0