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
124532372 12453237 2 F 2016 20160628 20160609 20160706 EXP US-SA-2016SA106237 AVENTIS 57.00 YR A F Y 0.00000 20160706 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
124532372 12453237 1 PS APIDRA SOLOSTAR INSULIN GLULISINE 1 Unknown 10 UNITS PLUS SSI 5F323A 21629 SOLUTION FOR INJECTION TID
124532372 12453237 2 SS SOLOSTAR DEVICE 1 5F323A 0 TID
124532372 12453237 3 C LANTUS INSULIN GLARGINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124532372 12453237 1 Type 2 diabetes mellitus
124532372 12453237 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124532372 12453237 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124532372 12453237 Blood glucose increased
124532372 12453237 Cataract
124532372 12453237 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
124532372 12453237 1 201603 0
124532372 12453237 2 201603 0