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
127764691 12776469 1 I 2002 20160912 20160923 20160923 EXP US-ELI_LILLY_AND_COMPANY-US201609004562 ELI LILLY AND CO 0.00 M Y 0.00000 20160923 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
127764691 12776469 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 16 U, UNKNOWN 18780 16 IU INJECTION
127764691 12776469 2 SS HUMULIN N INSULIN HUMAN 1 18780 INJECTION
127764691 12776469 3 SS HUMULIN R INSULIN HUMAN 1 Unknown 3 U, QD 0 3 IU INJECTION QD
127764691 12776469 4 SS HUMULIN R INSULIN HUMAN 1 0 INJECTION
127764691 12776469 5 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown UNK, UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127764691 12776469 1 Type 2 diabetes mellitus
127764691 12776469 2 Type 1 diabetes mellitus
127764691 12776469 3 Type 1 diabetes mellitus
127764691 12776469 4 Type 2 diabetes mellitus
127764691 12776469 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127764691 12776469 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127764691 12776469 Blood insulin decreased
127764691 12776469 Cardiac disorder
127764691 12776469 Hernia
127764691 12776469 Incorrect drug administration duration
127764691 12776469 Renal impairment
127764691 12776469 Renal mass

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
127764691 12776469 1 2004 0
127764691 12776469 3 2004 0