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
123010952 12301095 2 F 2007 20160707 20160425 20160715 EXP CA-BAYER-2016-072657 BAYER 55.00 YR A M Y 0.00000 20160715 CN CA CA

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
123010952 12301095 1 PS BETASERON INTERFERON BETA-1B 1 Subcutaneous 250 ML, UNK N 103471 250 ML POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
123010952 12301095 2 C ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 UNK 0
123010952 12301095 3 C IBUPROFEN. IBUPROFEN 1 UNK 0
123010952 12301095 4 C DUTASTERIDE. DUTASTERIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123010952 12301095 1 Secondary progressive multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
123010952 12301095 OT
123010952 12301095 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123010952 12301095 Benign prostatic hyperplasia
123010952 12301095 Localised infection
123010952 12301095 Multiple sclerosis

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
123010952 12301095 1 20000616 20160531 0