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
85450972 8545097 2 F 20111223 20111227 20120315 20120426 PER PHHY2011US13178 NOVARTIS 52.00 YR F N 96.60000 KG 20120306 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
85450972 8545097 1 PS GILENYA 1 ORAL 22527 0.5 MG QD
85450972 8545097 3 C ADVIL (MEFENAMIC ACID) 1 0
85450972 8545097 5 C DARVOCET-N (DEXTROPROPOXYPHENE NAPSILATE, PARACETAMOL) 2 0
85450972 8545097 7 C KLONOPIN (CLONAZEPAM) 2 0
85450972 8545097 9 C FLEXERIL (CYCLOBENZAPRINE HYDROCHLORIDE) 1 0
85450972 8545097 11 C LASIX (FUROSEMIDE) 1 0
85450972 8545097 13 C DEPAKOTE (VALPROATE SEMISODIUM) 2 0
85450972 8545097 15 C GLUCOPHAGE (METFORMIN) 2 0
85450972 8545097 17 C VIMPAT (LACOSAMIDE) 2 0
85450972 8545097 19 C LUNESTA (ESZOPICLONE) 2 0
85450972 8545097 21 C TYLENOL (PARACETAMOL) 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
85450972 8545097 1 MULTIPLE SCLEROSIS

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
85450972 8545097 Chest discomfort
85450972 8545097 Malaise
85450972 8545097 Muscle spasms
85450972 8545097 Oedema peripheral

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

Event ID CASEID RPSR COD
85450972 8545097 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
85450972 8545097 1 20110131 0