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
115503643 11550364 3 F 20121217 20160801 20150903 20160822 PER US-ELI_LILLY_AND_COMPANY-US201212007184 ELI LILLY AND CO 74.54 YR M Y 0.00000 20160822 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
115503643 11550364 1 PS HUMALOG INSULIN LISPRO 1 UNK, PRN U U 20563 INJECTION
115503643 11550364 2 SS HUMALOG INSULIN LISPRO 1 UNK, PRN U U C003016A 20563 INJECTION
115503643 11550364 3 SS HUMALOG INSULIN LISPRO 1 30 U, QD U U 20563 30 IU INJECTION QD
115503643 11550364 4 C LANTUS INSULIN GLARGINE 1 U 0
115503643 11550364 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115503643 11550364 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
115503643 11550364 Anxiety
115503643 11550364 Blood glucose decreased
115503643 11550364 Cataract
115503643 11550364 Drug dose omission
115503643 11550364 Hypokinesia
115503643 11550364 Incorrect dose administered
115503643 11550364 Neuropathy peripheral
115503643 11550364 Sensory loss

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
115503643 11550364 1 2006 0