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
89770163 8977016 3 F 2007 20160825 20121220 20160830 EXP BR-ELI_LILLY_AND_COMPANY-BR201211008916 ELI LILLY AND CO 0.00 M Y 100.00000 KG 20160830 CN BR BR

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
89770163 8977016 1 PS HUMULIN N INSULIN HUMAN 1 Subcutaneous 14 IU, QD BEFORE BRAKFEST 18780 14 IU INJECTION QD
89770163 8977016 2 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 14 IU, QD BEFORE LUNCH 18780 14 IU INJECTION QD
89770163 8977016 3 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 10 IU, QD BEFORE DINNER 18780 10 IU INJECTION QD
89770163 8977016 4 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous UNK, TID 0 INJECTION TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89770163 8977016 1 Type 2 diabetes mellitus
89770163 8977016 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
89770163 8977016 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89770163 8977016 Blood glucose fluctuation
89770163 8977016 Diabetic retinopathy
89770163 8977016 Drug dose omission
89770163 8977016 Hyperglycaemia
89770163 8977016 Visual impairment

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
89770163 8977016 4 1997 0