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
126233081 12623308 1 I 20160726 20160804 20160804 EXP US-SA-2016SA137793 AVENTIS 82.00 YR E F Y 0.00000 20160804 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
126233081 12623308 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:38 UNIT(S) UNK 21081 QD
126233081 12623308 2 C SOLOSTAR DEVICE 1 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126233081 12623308 1 Type 2 diabetes mellitus
126233081 12623308 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126233081 12623308 DS
126233081 12623308 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126233081 12623308 Blood glucose abnormal
126233081 12623308 Condition aggravated
126233081 12623308 Hydronephrosis
126233081 12623308 Macular degeneration
126233081 12623308 Nephrolithiasis
126233081 12623308 Sepsis
126233081 12623308 Septic shock
126233081 12623308 Urethral obstruction
126233081 12623308 Visual impairment

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

no results found

Therapies reported

no results found