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
126574921 12657492 1 I 201605 20160808 20160816 20160816 PER US-ELI_LILLY_AND_COMPANY-US201608005774 ELI LILLY AND CO 52.80 YR F Y 0.00000 20160816 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
126574921 12657492 1 PS HUMALOG INSULIN LISPRO 1 Unknown 8 U, QD, BEFORE BREAKFAST C572618E 20563 8 IU INJECTION QD
126574921 12657492 2 SS HUMALOG INSULIN LISPRO 1 Unknown 9 U, QD BEFORE LUNCH C572618E 20563 9 IU INJECTION QD
126574921 12657492 3 SS HUMALOG INSULIN LISPRO 1 Unknown 14 U, QD BEFORE DINNER C572618E 20563 14 IU INJECTION QD
126574921 12657492 4 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, PRN 20563 INJECTION
126574921 12657492 5 C LANTUS INSULIN GLARGINE 1 62 U, QD U U 0 62 IU QD
126574921 12657492 6 C METFORMIN METFORMIN HYDROCHLORIDE 1 1000 MG, BID U U 0 1000 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126574921 12657492 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126574921 12657492 Blood glucose increased
126574921 12657492 Dizziness
126574921 12657492 Dry mouth
126574921 12657492 Glycosylated haemoglobin increased
126574921 12657492 Incorrect dose administered
126574921 12657492 Malaise

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
126574921 12657492 1 201512 0
126574921 12657492 2 201512 0
126574921 12657492 3 201512 0
126574921 12657492 4 201512 0