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
127573111 12757311 1 I 20160824 20160829 20160919 20160919 PER US-009507513-1608USA014922 MERCK 67.38 YR M Y 0.00000 20160919 CN US 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
127573111 12757311 1 PS ZETIA EZETIMIBE 1 Oral 10 MG/ ONE A NIGHT 20 MG Y 21445 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127573111 12757311 1 Blood cholesterol

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127573111 12757311 Gait disturbance
127573111 12757311 Pain

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
127573111 12757311 1 20160823 20160827 0