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
125285711 12528571 1 I 2009 20160628 20160705 20160705 EXP US-ELI_LILLY_AND_COMPANY-US201606011163 ELI LILLY AND CO 63.89 YR M Y 0.00000 20160701 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
125285711 12528571 1 PS HUMALOG INSULIN LISPRO 1 Unknown 10 U, QID C558448A 20563 10 IU INJECTION QID
125285711 12528571 2 C LANTUS INSULIN GLARGINE 1 Unknown 30 U, EACH MORNING U 0 30 IU QD
125285711 12528571 3 C LANTUS INSULIN GLARGINE 1 Unknown 10 U, EACH EVENING U 0 10 IU QD
125285711 12528571 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125285711 12528571 1 Type 2 diabetes mellitus
125285711 12528571 2 Product used for unknown indication
125285711 12528571 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125285711 12528571 LT
125285711 12528571 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125285711 12528571 Blood glucose decreased
125285711 12528571 Blood glucose increased
125285711 12528571 Dizziness
125285711 12528571 Dyspnoea
125285711 12528571 Feeling abnormal
125285711 12528571 Lung infiltration
125285711 12528571 Myocardial infarction

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
125285711 12528571 1 2008 0