The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
4330776 4120984 I 4330776-3 20030901 20040316 20040331 EXP US_020181028 ELI LILLY AND COMPANY 56 YR M N 20040324

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
4330776 1004757071 PS HUMALOG 1 D 5MH75M 20030601 20563
4330776 1004766295 SS HUMULIN N 1 75 U/DAY D 5NA90N 20031101
4330776 1004766296 C FENTANYL 1
4330776 1004766298 C LANTUS 1
4330776 1004766299 C GLUCOVANCE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4330776 1004757071 DIABETES MELLITUS
4330776 1004766295 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
4330776 HO

Reactions reported

Event ID PT
4330776 AMNESIA
4330776 BLOOD GLUCOSE DECREASED
4330776 BLOOD GLUCOSE INCREASED
4330776 CORONARY ARTERY SURGERY
4330776 DIABETIC FOOT
4330776 FLUID RETENTION
4330776 HYPERHIDROSIS
4330776 MYOCARDIAL INFARCTION
4330776 PAIN
4330776 PHARMACEUTICAL PRODUCT COMPLAINT
4330776 SPINAL CORD INJURY
4330776 THYROID DISORDER
4330776 TREMOR
4330776 WEIGHT INCREASED

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4330776 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4330776 1004757071 20030901
4330776 1004766295 20000101 20030901