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
125802251 12580225 1 I 20160712 20160721 20160721 EXP US-SA-2016SA129370 AVENTIS 54.00 YR A M Y 0.00000 20160721 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
125802251 12580225 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown U 5F2205A 21081 QD
125802251 12580225 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:50 UNIT(S) U 5F2205A 21081 QD
125802251 12580225 3 C SOLOSTAR DEVICE 1 5F2205A 0 QD
125802251 12580225 4 C SOLOSTAR DEVICE 1 5F2205A 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125802251 12580225 1 Type 2 diabetes mellitus
125802251 12580225 2 Type 2 diabetes mellitus
125802251 12580225 3 Type 2 diabetes mellitus
125802251 12580225 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125802251 12580225 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125802251 12580225 Arthralgia
125802251 12580225 Blood glucose decreased
125802251 12580225 Headache
125802251 12580225 Hypoaesthesia
125802251 12580225 Nasal discomfort
125802251 12580225 Staphylococcal infection
125802251 12580225 Toothache

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found