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
118869643 11886964 3 F 20150917 20160201 20160104 20160210 EXP PL-BIOGEN-2015BI128377 BIOGEN 43.00 YR M Y 93.50000 KG 20160210 MD PL PL

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
118869643 11886964 1 PS BG00012 DIMETHYL FUMARATE 1 Oral 73061 PROLONGED-RELEASE CAPSULE BID
118869643 11886964 2 C EUTHYROX LEVOTHYROXINE SODIUM 1 Oral 0 100 UG
118869643 11886964 3 C EUTHYROX LEVOTHYROXINE SODIUM 1 Oral 0 112 UG TIW
118869643 11886964 4 C DORETA 2 Oral 0 QD
118869643 11886964 5 C STILNOX ZOLPIDEM TARTRATE 1 Oral 0 10 MG
118869643 11886964 6 C CIPRONEX CIPROFLOXACIN 1 Oral 0 500 MG BID
118869643 11886964 7 C CIPRONEX CIPROFLOXACIN 1 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118869643 11886964 1 Multiple sclerosis
118869643 11886964 2 Hypothyroidism
118869643 11886964 4 Analgesic therapy
118869643 11886964 5 Insomnia
118869643 11886964 6 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
118869643 11886964 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118869643 11886964 Nephrolithiasis
118869643 11886964 Renal colic
118869643 11886964 Ureterolithiasis

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
118869643 11886964 1 20150723 0
118869643 11886964 2 200903 0
118869643 11886964 3 200903 0
118869643 11886964 4 20141120 0
118869643 11886964 5 2010 0
118869643 11886964 6 20150915 0