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
128003631 12800363 1 I 2016 20160922 20160930 20160930 EXP US-ELI_LILLY_AND_COMPANY-US201609008836 ELI LILLY AND CO 38.00 YR M Y 0.00000 20160930 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
128003631 12800363 1 PS Insulin Human INSULIN HUMAN 1 Unknown UNK UNK, UNKNOWN U U C524367A 18780 INJECTION
128003631 12800363 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN U U 0
128003631 12800363 3 SS NOVOLOG INSULIN ASPART 1 Unknown UNK, UNKNOWN U U 0
128003631 12800363 4 SS LANTUS INSULIN GLARGINE 1 Unknown UNK, UNKNOWN U U 0
128003631 12800363 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
128003631 12800363 1 Diabetes mellitus
128003631 12800363 2 Product used for unknown indication
128003631 12800363 3 Product used for unknown indication
128003631 12800363 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
128003631 12800363 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
128003631 12800363 Blood glucose increased
128003631 12800363 Lymphoedema

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
128003631 12800363 1 20160622 0