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
126378121 12637812 1 I 20160801 20160809 20160809 EXP CN-ELI_LILLY_AND_COMPANY-CN201608001603 ELI LILLY AND CO 70.00 YR F Y 0.00000 20160809 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
126378121 12637812 1 PS HUMULIN R INSULIN HUMAN 1 Subcutaneous UNK, UNKNOWN 18780 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126378121 12637812 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126378121 12637812 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126378121 12637812 Blood glucose increased
126378121 12637812 Diabetic complication
126378121 12637812 Dizziness
126378121 12637812 Hypoglycaemia
126378121 12637812 Influenza

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
126378121 12637812 1 2008 0