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
123186403 12318640 3 F 20160826 20160429 20160906 EXP US-SA-2016SA083353 AVENTIS 66.00 YR E F Y 85.70000 KG 20160906 PH 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
123186403 12318640 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:35 UNIT(S) 5F2472A 21081 INJECTION QD
123186403 12318640 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:70 UNIT(S) 5F2472A 21081 INJECTION QD
123186403 12318640 3 C SOLOSTAR DEVICE 1 0 QD
123186403 12318640 4 C RAMIPRIL. RAMIPRIL 1 0
123186403 12318640 5 C GABAPENTIN. GABAPENTIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123186403 12318640 1 Type 2 diabetes mellitus
123186403 12318640 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
123186403 12318640 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123186403 12318640 Amnesia
123186403 12318640 Blood glucose increased
123186403 12318640 Blood sodium decreased
123186403 12318640 Incorrect product storage
123186403 12318640 Trigeminal neuralgia
123186403 12318640 Urinary tract infection

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

no results found

Therapies reported

no results found