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
126520301 12652030 1 I 2012 20160801 20160815 20160815 PER US-ELI_LILLY_AND_COMPANY-US201608006701 ELI LILLY AND CO 52.97 YR M Y 0.00000 20160815 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
126520301 12652030 1 PS HUMALOG INSULIN LISPRO 1 Unknown 15 U, QID, PLUS SLIDING SCALE C467947E 20563 15 IU INJECTION QID
126520301 12652030 2 SS HUMALOG INSULIN LISPRO 1 Unknown 15 U, QID, PLUS SLIDING SCALE UNKNOWN 20563 15 IU INJECTION QID
126520301 12652030 3 C LEVEMIR INSULIN DETEMIR 1 Unknown UNK, UNKNOWN U 0
126520301 12652030 4 C TOUJEO INSULIN GLARGINE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126520301 12652030 1 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126520301 12652030 Blood glucose abnormal
126520301 12652030 Blood glucose increased
126520301 12652030 Drug dose omission
126520301 12652030 Injection site mass
126520301 12652030 Injury associated with device
126520301 12652030 Needle issue
126520301 12652030 Pruritus

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
126520301 12652030 1 201601 0
126520301 12652030 2 201601 0