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
127857691 12785769 1 I 2016 20160916 20160927 20160927 EXP AU-SA-2016SA172306 AVENTIS 0.00 A F Y 0.00000 20160927 CN AU AU

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
127857691 12785769 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) U UNKNOWN 21081 QD
127857691 12785769 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) U UNKNOWN 21081 QD
127857691 12785769 3 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) U UNKNOWN 21081 QD
127857691 12785769 4 C SOLOSTAR DEVICE 1 0
127857691 12785769 5 C NOVORAPID INSULIN ASPART 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127857691 12785769 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127857691 12785769 Blood glucose decreased
127857691 12785769 Injection site pain
127857691 12785769 Pancreatitis

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
127857691 12785769 1 2011 201508 0
127857691 12785769 2 2016 2016 0
127857691 12785769 3 201609 0
127857691 12785769 4 2011 0