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
127207801 12720780 1 I 201605 20160826 20160907 20160907 PER US-ELI_LILLY_AND_COMPANY-US201608012604 ELI LILLY AND CO 78.53 YR F Y 77.10000 KG 20160907 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
127207801 12720780 1 PS HUMULIN R INSULIN HUMAN 1 Subcutaneous 5 U, TID 18780 5 IU TID
127207801 12720780 2 SS LEVEMIR INSULIN DETEMIR 1 Unknown 28 U, QD 0 28 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127207801 12720780 1 Type 2 diabetes mellitus
127207801 12720780 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127207801 12720780 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127207801 12720780 Abdominal pain upper
127207801 12720780 Back pain
127207801 12720780 Blood glucose decreased
127207801 12720780 Headache
127207801 12720780 Hypoglycaemic unconsciousness
127207801 12720780 Vision blurred
127207801 12720780 Weight increased

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
127207801 12720780 1 201605 0
127207801 12720780 2 201605 0