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
126235151 12623515 1 I 20160520 20160722 20160804 20160804 EXP FR-ECLAT PHARMACEUTICALS-2016ECL00020 ECLAT 87.00 YR F Y 0.00000 20160804 CN US FR

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
126235151 12623515 1 PS PARIET RABEPRAZOLE SODIUM 1 Oral 20 MG, 1X/DAY Y U 204736 20 MG TABLET QD
126235151 12623515 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral UNK Y 0
126235151 12623515 3 C CACIT VITAMIN D3 CALCIUM CARBONATECHOLECALCIFEROL 1 0
126235151 12623515 4 C DOLIPRANE ACETAMINOPHEN 1 0
126235151 12623515 5 C MIOREL THIOCOLCHICOSIDE 1 0
126235151 12623515 6 SS ALDACTAZINE ALTHIAZIDESPIRONOLACTONE 1 UNK Y 0
126235151 12623515 7 SS LEVOTHYROXINE. LEVOTHYROXINE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126235151 12623515 HO
126235151 12623515 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126235151 12623515 Fall
126235151 12623515 Hyponatraemia

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
126235151 12623515 1 20160520 0
126235151 12623515 2 20160506 20160524 0
126235151 12623515 6 20160506 20160524 0