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
125062712 12506271 2 F 20160616 20160713 20160628 20160721 PER US-ELI_LILLY_AND_COMPANY-US201606008566 ELI LILLY AND CO 0.00 F Y 0.00000 20160721 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
125062712 12506271 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK, OTHER C506924G 20563 INJECTION
125062712 12506271 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK UNK, OTHER C405605F 0 INJECTION
125062712 12506271 3 C LANTUS INSULIN GLARGINE 1 U 0
125062712 12506271 4 C LEVEMIR INSULIN DETEMIR 1 U 0
125062712 12506271 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 U 0
125062712 12506271 6 C TOUJEO INSULIN GLARGINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125062712 12506271 1 Type 1 diabetes mellitus
125062712 12506271 2 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125062712 12506271 Blood glucose increased
125062712 12506271 Incorrect dose administered

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
125062712 12506271 1 20160612 0
125062712 12506271 2 201606 0