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
127688211 12768821 1 I 20160908 20160921 20160921 PER US-ELI_LILLY_AND_COMPANY-US201609003723 ELI LILLY AND CO 0.00 F Y 0.00000 20160921 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
127688211 12768821 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 15 U, PRN 18780 15 IU INJECTION
127688211 12768821 2 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown UNK, UNKNOWN U U C533327D 0 INJECTION
127688211 12768821 3 C NOVOLOG INSULIN ASPART 1 5 U, PRN 0 5 IU

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127688211 12768821 1 Type 2 diabetes mellitus
127688211 12768821 2 Product used for unknown indication
127688211 12768821 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127688211 12768821 Blood glucose abnormal
127688211 12768821 Glycosylated haemoglobin increased
127688211 12768821 Nasopharyngitis

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
127688211 12768821 1 20160708 0