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
123107404 12310740 4 F 2014 20160829 20160427 20160909 EXP US-ELI_LILLY_AND_COMPANY-US201604001268 ELI LILLY AND CO 62.90 YR F Y 115.20000 KG 20160909 MD 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
123107404 12310740 1 PS HUMULIN R INSULIN HUMAN 1 Unknown 24 U, EACH MORNING C477811A 18780 24 IU INJECTION QD
123107404 12310740 2 SS HUMULIN R INSULIN HUMAN 1 Unknown 20 U, EACH EVENING C477811A 18780 20 IU INJECTION QD
123107404 12310740 3 SS HUMULIN R INSULIN HUMAN 1 Unknown RAISE OR LOWER HER DOSAGE A LITTLE 18780 INJECTION
123107404 12310740 4 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 38 U, BEFORE BED U U C464897D 0 38 IU INJECTION
123107404 12310740 5 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK UNK, UNKNOWN U U 0 INJECTION
123107404 12310740 6 SS HUMULIN R U-500 INSULIN HUMAN 1 Unknown 145 U, EACH MORNING U U C509906E 0 145 IU INJECTION QD
123107404 12310740 7 SS HUMULIN R U-500 INSULIN HUMAN 1 Unknown 95 U, AT SUPPER TIME U U C509906E 0 95 IU INJECTION
123107404 12310740 8 SS HUMULIN R U-500 INSULIN HUMAN 1 Unknown 135 U, EACH MORNING U U 0 135 IU INJECTION QD
123107404 12310740 9 SS HUMULIN R U-500 INSULIN HUMAN 1 Unknown 95 U, EACH EVENING U U 0 95 IU INJECTION QD
123107404 12310740 10 SS COUMADIN WARFARIN SODIUM 1 Unknown UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123107404 12310740 1 Type 2 diabetes mellitus
123107404 12310740 2 Insulin resistance
123107404 12310740 4 Type 2 diabetes mellitus
123107404 12310740 6 Type 2 diabetes mellitus
123107404 12310740 10 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
123107404 12310740 HO
123107404 12310740 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123107404 12310740 Anaemia
123107404 12310740 Asthma
123107404 12310740 Atrial fibrillation
123107404 12310740 Blood glucose decreased
123107404 12310740 Blood glucose increased
123107404 12310740 Drug dose omission
123107404 12310740 Haemorrhage
123107404 12310740 Hepatic cirrhosis
123107404 12310740 Neuropathy peripheral
123107404 12310740 Varices oesophageal

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
123107404 12310740 1 1996 201605 0
123107404 12310740 2 1996 201605 0
123107404 12310740 4 201605 20160823 0
123107404 12310740 5 20160829 0
123107404 12310740 6 201605 0
123107404 12310740 7 201605 0