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
126908961 12690896 1 I 20160815 20160826 20160826 EXP CN-ELI_LILLY_AND_COMPANY-CN201608008924 ELI LILLY AND CO 0.00 F Y 0.00000 20160825 CN CN CN

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
126908961 12690896 1 PS HUMULIN 70/30 INSULIN HUMAN 1 Subcutaneous UNK, UNKNOWN 18780 INJECTION
126908961 12690896 2 SS HUMULIN 70/30 INSULIN HUMAN 1 Subcutaneous UNK, UNKNOWN 18780 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126908961 12690896 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126908961 12690896 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126908961 12690896 Blood glucose abnormal
126908961 12690896 Blood glucose increased
126908961 12690896 Drug ineffective

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

no results found

Therapies reported

no results found