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
126340831 12634083 1 I 201003 20100510 20160809 20160809 EXP US-GLAXOSMITHKLINE-A0858947A GLAXOSMITHKLINE 52.25 YR F Y 0.00000 20160809 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
126340831 12634083 1 PS LOVAZA OMEGA-3-ACID ETHYL ESTERS 1 Oral 2 DF, BID U UNKNOWN 21654 2 DF CAPSULE BID
126340831 12634083 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 U 0
126340831 12634083 3 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0
126340831 12634083 4 C CITRACAL CALCIUM CITRATE 1 U 0
126340831 12634083 5 C GLUCOSAMINE GLUCOSAMINE 1 U 0
126340831 12634083 6 C VITAMIN C ASCORBIC ACID 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126340831 12634083 1 Blood triglycerides increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126340831 12634083 Flatulence
126340831 12634083 Laboratory test abnormal
126340831 12634083 Product substitution issue
126340831 12634083 Therapeutic response changed
126340831 12634083 Therapeutic response decreased

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
126340831 12634083 1 201002 0