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
124335102 12433510 2 F 2008 20160720 20160603 20160729 EXP US-SA-2016SA104109 AVENTIS 77.00 YR E F Y 85.28000 KG 20160729 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
124335102 12433510 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:20 UNIT(S) 5F2398A 21081 BID
124335102 12433510 2 C SOLOSTAR DEVICE 1 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124335102 12433510 1 Type 2 diabetes mellitus
124335102 12433510 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124335102 12433510 HO
124335102 12433510 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124335102 12433510 Cataract
124335102 12433510 Hospitalisation
124335102 12433510 Product use issue
124335102 12433510 Visual impairment
124335102 12433510 Wrong technique in product usage process

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
124335102 12433510 1 2008 0
124335102 12433510 2 2008 0