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
126987652 12698765 2 F 20140820 20160822 20160830 20160901 EXP US-SA-2016SA155890 AVENTIS 73.00 YR E F Y 0.00000 20160901 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
126987652 12698765 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE:55 UNIT(S) 6F2811A 21081 BID
126987652 12698765 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE:100 UNIT(S) UNK 21081 QD
126987652 12698765 3 C SOLOSTAR DEVICE 1 Subcutaneous 6F2811A 0 BID
126987652 12698765 4 C SOLOSTAR DEVICE 1 Subcutaneous UNK 0 QD
126987652 12698765 5 C HUMALOG INSULIN LISPRO 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126987652 12698765 1 Type 2 diabetes mellitus
126987652 12698765 2 Type 2 diabetes mellitus
126987652 12698765 3 Type 2 diabetes mellitus
126987652 12698765 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126987652 12698765 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126987652 12698765 Blood glucose increased
126987652 12698765 Cerebrovascular accident
126987652 12698765 Dysarthria
126987652 12698765 Product use issue

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

no results found

Therapies reported

no results found