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
126268871 12626887 1 I 20160725 20160805 20160805 EXP KR-ELI_LILLY_AND_COMPANY-KR201607011410 ELI LILLY AND CO 0.00 M Y 0.00000 20160805 CN KR KR

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
126268871 12626887 1 PS HUMULIN N INSULIN HUMAN 1 Unknown SLIDING SCALE AT 6 AM 18780 56 IU INJECTION QD
126268871 12626887 2 SS HUMULIN N INSULIN HUMAN 1 Unknown SLIDING SCALE AT 6 AM 18780 60 IU INJECTION QD
126268871 12626887 3 SS HUMULIN N INSULIN HUMAN 1 Unknown SLIDING SCALE AT 12 PM 18780 12 IU INJECTION QD
126268871 12626887 4 SS HUMULIN N INSULIN HUMAN 1 Unknown SLIDING SCALE AT 12 PM 18780 14 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126268871 12626887 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126268871 12626887 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126268871 12626887 Altered state of consciousness
126268871 12626887 Anxiety
126268871 12626887 Asthenia
126268871 12626887 Blood glucose decreased
126268871 12626887 Blood glucose increased
126268871 12626887 Cardiac disorder
126268871 12626887 Fatigue

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
126268871 12626887 1 2006 0
126268871 12626887 2 2006 0
126268871 12626887 3 2006 0