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
125221411 12522141 1 I 2015 20160621 20160701 20160701 EXP US-SA-2016SA117702 AVENTIS 57.00 YR A F Y 0.00000 20160701 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
125221411 12522141 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:55 UNIT(S) UNK 21081 INJECTION QD
125221411 12522141 2 C SOLOSTAR DEVICE 1 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125221411 12522141 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125221411 12522141 HO
125221411 12522141 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125221411 12522141 Blindness unilateral
125221411 12522141 Blood pressure increased
125221411 12522141 Cerebrovascular accident
125221411 12522141 Headache
125221411 12522141 Limb malformation
125221411 12522141 Product supply issue
125221411 12522141 Tremor
125221411 12522141 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
125221411 12522141 1 2013 0
125221411 12522141 2 2013 0