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
127805681 12780568 1 I 20160912 20160926 20160926 EXP CN-ELI_LILLY_AND_COMPANY-CN201609004602 ELI LILLY AND CO 0.00 F Y 0.00000 20160920 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
127805681 12780568 1 PS HUMULIN R INSULIN HUMAN 1 Subcutaneous UNK, UNKNOWN Y U 18780 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127805681 12780568 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127805681 12780568 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127805681 12780568 Hypoglycaemia
127805681 12780568 Syncope

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

no results found

Therapies reported

no results found