The Safety Rates Drug Report

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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
88766133 8876613 3 F 20120209 20120918 20120426 20130107 PER PHEH2012US003926 NOVARTIS 48.00 YR F N 74.80000 KG 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
88766133 8876613 1 PS GILENYA (FTY) CAPSULE, 0.5MG 1 ORAL D D S0010B 20130220 22527 0.5 MG QD
88766133 8876613 3 C RITALIN 1 0
88766133 8876613 5 C ZOLOFT (SERTRALINE HYDROCHLORIDE) 1 0
88766133 8876613 7 C VICODIN (HYDROCODONE BITARTRATE, PARACETAMOL) 2 0
88766133 8876613 9 C SOMA (CARISOPRODOL) 2 0
88766133 8876613 11 C ACIPHEX (RABEPRAZOLE SODIUM) 1 0
88766133 8876613 13 C GABAPENTIN 1 0
88766133 8876613 15 C FOCALIN (DEXMETHYLPHENIDATE HYDROCHLORIDE) 2 0
88766133 8876613 17 C AMITRIPTYLINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88766133 8876613 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
88766133 8876613 Diarrhoea
88766133 8876613 Dysphonia
88766133 8876613 Headache
88766133 8876613 Hyperhidrosis
88766133 8876613 Oropharyngeal pain
88766133 8876613 Visual impairment

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

Event ID CASEID RPSR COD
88766133 8876613 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
88766133 8876613 1 20120207 0