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
112182692 11218269 2 F 2014 20160707 20150625 20160715 EXP US-SA-2015SA089926 AVENTIS 71.00 YR E M Y 112.00000 KG 20160715 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
112182692 11218269 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:26 UNIT(S) UNK 21081 INJECTION QD
112182692 11218269 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:28 UNIT(S) UNK 21081 INJECTION QD
112182692 11218269 3 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:26 UNIT(S) UNK 21081 INJECTION QD
112182692 11218269 4 C SOLOSTAR DEVICE 1 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112182692 11218269 1 Diabetes mellitus
112182692 11218269 2 Diabetes mellitus
112182692 11218269 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
112182692 11218269 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112182692 11218269 Back pain
112182692 11218269 Blood glucose decreased
112182692 11218269 Condition aggravated
112182692 11218269 Drug ineffective
112182692 11218269 Leukaemia
112182692 11218269 Nausea
112182692 11218269 Spinal disorder
112182692 11218269 Visual impairment

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

no results found

Therapies reported

no results found