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
110838622 11083862 2 F 201405 20160816 20150501 20160823 EXP US-ELI_LILLY_AND_COMPANY-US201504007087 ELI LILLY AND CO 31.84 YR F Y 65.76000 KG 20160823 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
110838622 11083862 1 PS HUMALOG INSULIN LISPRO 1 Subcutaneous 40 U, QD 20563 40 IU INJECTION QD
110838622 11083862 2 C PRENATAL /00231801/ VITAMINS 1 U 0
110838622 11083862 3 C VITAMIN D /00107901/ ERGOCALCIFEROL 1 U 0
110838622 11083862 4 C FOLIC ACID. FOLIC ACID 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110838622 11083862 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
110838622 11083862 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110838622 11083862 Blood glucose decreased
110838622 11083862 Blood glucose increased
110838622 11083862 Blood pressure decreased
110838622 11083862 Exposure during breast feeding
110838622 11083862 Insulin resistance
110838622 11083862 Maternal exposure during pregnancy
110838622 11083862 Oedema peripheral

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
110838622 11083862 1 1990 0