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
100647257 10064725 7 F 2014 20160706 20140408 20160714 EXP US-SA-2014SA039396 AVENTIS 54.00 YR A M Y 0.00000 20160714 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
100647257 10064725 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE:66 UNIT(S) 3F083A 21081 QD
100647257 10064725 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE:66 UNIT(S) 21081 QD
100647257 10064725 3 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE:65 UNIT(S) 5F1585A 21081 QD
100647257 10064725 4 C SOLOSTAR DEVICE 1 Subcutaneous 3F083A 0 QD
100647257 10064725 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100647257 10064725 1 Type 2 diabetes mellitus
100647257 10064725 2 Type 2 diabetes mellitus
100647257 10064725 3 Type 2 diabetes mellitus
100647257 10064725 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
100647257 10064725 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100647257 10064725 Condition aggravated
100647257 10064725 Cough
100647257 10064725 Drug dose omission
100647257 10064725 Eye haemorrhage
100647257 10064725 Lacrimation increased
100647257 10064725 Nasal congestion
100647257 10064725 Nasopharyngitis
100647257 10064725 Vision blurred

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
100647257 10064725 1 2012 0
100647257 10064725 2 2012 0
100647257 10064725 3 20100710 0
100647257 10064725 4 2012 0