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
127386551 12738655 1 I 2016 20160809 20160912 20160912 PER US-SA-2016SA147420 AVENTIS 47.00 YR A M Y 0.00000 20160912 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
127386551 12738655 1 PS TOUJEO INSULIN GLARGINE 1 Unknown DOSE:22 UNIT(S) 6F293A 206538 QD
127386551 12738655 2 SS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 Unknown U UNKNOWN 0
127386551 12738655 3 SS LISINOPRIL. LISINOPRIL 1 Unknown U UNKNOWN 0
127386551 12738655 4 SS LISINOPRIL. LISINOPRIL 1 Unknown U UNKNOWN 0
127386551 12738655 5 C SOLOSTAR DEVICE 1 0
127386551 12738655 6 C NOVOLIN R INSULIN HUMAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127386551 12738655 1 Type 2 diabetes mellitus
127386551 12738655 2 Blood pressure measurement
127386551 12738655 3 Blood pressure measurement
127386551 12738655 4 Blood pressure measurement

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127386551 12738655 Anxiety
127386551 12738655 Blood glucose increased
127386551 12738655 Blood pressure increased
127386551 12738655 Fluid retention
127386551 12738655 Heart rate increased
127386551 12738655 Weight increased

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
127386551 12738655 1 201607 0
127386551 12738655 2 20160719 0
127386551 12738655 3 20160717 0
127386551 12738655 5 201607 0