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
125983781 12598378 1 I 20160718 20160727 20160727 PER US-ELI_LILLY_AND_COMPANY-US201607007331 ELI LILLY AND CO 0.00 M Y 0.00000 20160727 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
125983781 12598378 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 18 U, BID 18780 18 IU INJECTION BID
125983781 12598378 2 SS HUMULIN N INSULIN HUMAN 1 Unknown 18 U, BID C215885A 18780 18 IU INJECTION BID
125983781 12598378 3 SS HUMULIN R INSULIN HUMAN 1 Unknown 18 U, BID 0 18 IU INJECTION BID
125983781 12598378 4 SS HUMULIN R INSULIN HUMAN 1 Unknown 18 U, BID C494916E 0 18 IU INJECTION BID
125983781 12598378 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125983781 12598378 1 Type 1 diabetes mellitus
125983781 12598378 3 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125983781 12598378 Blood glucose increased
125983781 12598378 Drug ineffective
125983781 12598378 Intentional product misuse

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found