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
126718391 12671839 1 I 20141231 20160818 20160822 20160822 EXP US-GLAXOSMITHKLINE-US2016120262 GLAXOSMITHKLINE 62.67 YR F Y 0.00000 20160822 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
126718391 12671839 1 PS LOVAZA OMEGA-3-ACID ETHYL ESTERS 1 Oral 1 G, BID U 21654 1 G CAPSULE BID
126718391 12671839 2 SS LOVAZA OMEGA-3-ACID ETHYL ESTERS 1 U 21654 CAPSULE
126718391 12671839 3 SS OMEGA-3-ACID ETHYL ESTERS. OMEGA-3-ACID ETHYL ESTERS 1 Oral 1 G, BID Y 21654 1 G CAPSULE BID
126718391 12671839 4 SS OMEGA-3-ACID ETHYL ESTERS. OMEGA-3-ACID ETHYL ESTERS 1 Y 21654 CAPSULE
126718391 12671839 5 C BLACK ELDERBERRY 2 U 0
126718391 12671839 6 C COMBIGAN BRIMONIDINE TARTRATETIMOLOL MALEATE 1 U 0
126718391 12671839 7 C ECHINACEA AND GOLDENSEAL 2 U 0
126718391 12671839 8 C ESTER C 2 U 0
126718391 12671839 9 C GLUCOSAMINE CHONDROITIN CHONDROITIN SULFATE (BOVINE)GLUCOSAMINE HYDROCHLORIDE 1 U 0
126718391 12671839 10 C TEA TEA LEAF 1 U 0
126718391 12671839 11 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0
126718391 12671839 12 C LUMIGAN BIMATOPROST 1 U 0
126718391 12671839 13 C MAGNESIUM MAGNESIUM 1 U 0
126718391 12671839 14 C OIL OF OREGANO 2 U 0
126718391 12671839 15 C RESVERATROL RESVERATROL 1 U 0
126718391 12671839 16 C VITAMIN D3 CHOLECALCIFEROL 1 U 0
126718391 12671839 17 C GEMFIBROZIL. GEMFIBROZIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126718391 12671839 1 Blood cholesterol increased
126718391 12671839 2 Blood triglycerides increased
126718391 12671839 3 Blood cholesterol increased
126718391 12671839 4 Blood triglycerides increased

Outcome of event

Event ID CASEID OUTC COD
126718391 12671839 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126718391 12671839 Dyspepsia
126718391 12671839 Glaucoma

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
126718391 12671839 3 201410 0