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
118367512 11836751 2 F 20160129 20151215 20160210 EXP US-SA-2015SA208362 AVENTIS 69.00 YR E M Y 0.00000 20160210 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
118367512 11836751 1 PS LANTUS INSULIN GLARGINE 1 Unknown DREQUENCY- DAILY MORNING DOSE:20 UNIT(S) A4837 21081 SOLUTION FOR INJECTION QD
118367512 11836751 2 C HUMALOG INSULIN LISPRO 1 DOSE: SLIDING SCALE 0
118367512 11836751 3 C CYCLOSPORIN CYCLOSPORINE 1 0 100 MG QD
118367512 11836751 4 C CYCLOSPORIN CYCLOSPORINE 1 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118367512 11836751 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
118367512 11836751 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118367512 11836751 Blood glucose abnormal
118367512 11836751 Blood glucose decreased
118367512 11836751 Cataract
118367512 11836751 Memory impairment
118367512 11836751 Product quality issue
118367512 11836751 Renal disorder
118367512 11836751 Visual impairment

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

no results found

Therapies reported

no results found