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
125552461 12555246 1 I 20160616 20160624 20160714 20160714 PER US-009507513-1606USA012970 MERCK 70.00 YR F Y 0.00000 20160714 MD 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
125552461 12555246 1 PS ZETIA EZETIMIBE 1 Oral 100 MG, UNK 21445 100 MG TABLET
125552461 12555246 2 C MIRAPEX PRAMIPEXOLE DIHYDROCHLORIDE 1 U 0
125552461 12555246 3 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 THYROID U 0
125552461 12555246 4 C VITAMIN D CHOLECALCIFEROL 1 U 0
125552461 12555246 5 C MAGNESIUM OXIDE. MAGNESIUM OXIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125552461 12555246 1 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125552461 12555246 Diarrhoea
125552461 12555246 General physical condition abnormal

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
125552461 12555246 1 20160609 0