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
126805352 12680535 2 F 20160831 20160824 20160906 PER US-ELI_LILLY_AND_COMPANY-US201608004793 ELI LILLY AND CO 0.00 M Y 0.00000 20160906 CN US US

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
126805352 12680535 1 PS HUMULIN R INSULIN HUMAN 1 Unknown 25 U, ON A SLIDING SCALE 18780 25 IU INJECTION
126805352 12680535 2 SS HUMULIN R INSULIN HUMAN 1 Unknown 25 U, ON A SLIDING SCALE C524366A 18780 25 IU INJECTION
126805352 12680535 3 SS HUMULIN R INSULIN HUMAN 1 Unknown 25 U, ON A SLIDING SCALE C524367A 18780 25 IU INJECTION
126805352 12680535 4 SS HUMULIN R U-500 INSULIN HUMAN 1 Unknown UNK, UNKNOWN U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126805352 12680535 1 Type 2 diabetes mellitus
126805352 12680535 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126805352 12680535 Blood glucose abnormal
126805352 12680535 Blood glucose decreased
126805352 12680535 Blood glucose fluctuation
126805352 12680535 Blood glucose increased
126805352 12680535 Drug dispensing error
126805352 12680535 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
126805352 12680535 1 2013 0