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
124960672 12496067 2 F 2009 20160628 20160624 20160706 EXP CN-ELI_LILLY_AND_COMPANY-CN201606007801 ELI LILLY AND CO 0.00 F Y 62.00000 KG 20160706 CN CN CN

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
124960672 12496067 1 PS HUMULIN R INSULIN HUMAN 1 Unknown UNK, UNKNOWN U U 18780 INJECTION
124960672 12496067 2 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 8 U, EACH MORNING U U 18780 8 IU INJECTION QD
124960672 12496067 3 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 8 U, AT NOON U U 18780 8 IU INJECTION QD
124960672 12496067 4 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 8 U, AT NOON U U 18780 8 IU INJECTION QD
124960672 12496067 5 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, UNKNOWN U U 0 INJECTION
124960672 12496067 6 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 17 U, EACH EVENING U U 0 17 IU INJECTION QD
124960672 12496067 7 C ACARBOSE. ACARBOSE 1 Unknown UNK, UNKNOWN U 0
124960672 12496067 8 C ASPIRIN /00002701/ ASPIRIN 1 Unknown UNK, UNKNOWN U 0
124960672 12496067 9 C SIMVASTATIN. SIMVASTATIN 1 Unknown UNK, UNKNOWN U 0
124960672 12496067 10 C CONCOR BISOPROLOL FUMARATE 1 Unknown UNK, UNKNOWN U 0
124960672 12496067 11 C ANBOL 2 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124960672 12496067 1 Diabetes mellitus
124960672 12496067 5 Diabetes mellitus
124960672 12496067 7 Product used for unknown indication
124960672 12496067 8 Product used for unknown indication
124960672 12496067 9 Product used for unknown indication
124960672 12496067 10 Product used for unknown indication
124960672 12496067 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124960672 12496067 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124960672 12496067 Blood glucose abnormal
124960672 12496067 Blood glucose decreased
124960672 12496067 Blood glucose increased
124960672 12496067 Diabetic ketoacidosis
124960672 12496067 Ear disorder
124960672 12496067 Peripheral swelling
124960672 12496067 Visual acuity reduced

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
124960672 12496067 1 2009 0
124960672 12496067 5 2009 0