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
125376421 12537642 1 I 20160610 20160701 20160707 20160707 PER US-ELI_LILLY_AND_COMPANY-US201607001415 ELI LILLY AND CO 68.27 YR M Y 0.00000 20160707 OT 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
125376421 12537642 1 PS HUMULIN R INSULIN HUMAN 1 Unknown 70 U, EACH MORNING UNKNOWN 18780 70 IU INJECTION QD
125376421 12537642 2 SS HUMULIN R INSULIN HUMAN 1 Unknown 70 U, EACH EVENING UNKNOWN 18780 70 IU INJECTION QD
125376421 12537642 3 SS HUMULIN R INSULIN HUMAN 1 Unknown 70 U, EACH MORNING C524365A 18780 70 IU INJECTION QD
125376421 12537642 4 SS HUMULIN R INSULIN HUMAN 1 Unknown 40 U, EACH EVENING C524365A 18780 40 IU INJECTION QD
125376421 12537642 5 C TRADJENTA LINAGLIPTIN 1 U 0
125376421 12537642 6 C GLIMEPIRIDE. GLIMEPIRIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125376421 12537642 1 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125376421 12537642 Blood glucose increased
125376421 12537642 Drug ineffective
125376421 12537642 Overweight

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
125376421 12537642 1 2015 0
125376421 12537642 2 2015 0