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
4873860 5938848 F 2 4873860-8 20051208 20060104 EXP USA050494672 ELI LILLY AND COMPANY 51 YR M N 62.3 KG 20051214 CN UNITED STATES

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
4873860 1006793567 PS HUMALOG 1 AS NEEDED D D 8RY10M 20060701 20563
4873860 1006821034 SS HUMULIN N 1 D D
4873860 1006821035 SS HUMULIN R 1 D D
4873860 1006821038 SS HUMULIN L 1 Y D
4873860 1006821054 SS LENTE ILETIN II 1 D D
4873860 1006821058 C LANTUS 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4873860 1006793567 DIABETES MELLITUS
4873860 1006821034 DIABETES MELLITUS INSULIN-DEPENDENT
4873860 1006821035 DIABETES MELLITUS INSULIN-DEPENDENT
4873860 1006821038 DIABETES MELLITUS INSULIN-DEPENDENT
4873860 1006821054 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
4873860 DS
4873860 OT

Reactions reported

Event ID PT
4873860 BLOOD GLUCOSE DECREASED
4873860 BLOOD GLUCOSE INCREASED
4873860 CONFUSIONAL STATE
4873860 CONVULSION
4873860 HYPERHIDROSIS
4873860 HYPERMETABOLISM
4873860 HYPOGLYCAEMIA
4873860 LOSS OF CONSCIOUSNESS
4873860 MOOD ALTERED
4873860 PHARMACEUTICAL PRODUCT COMPLAINT
4873860 TREMOR
4873860 WEIGHT GAIN POOR

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

Event ID RPSR COD
4873860 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4873860 1006793567 20030101
4873860 1006821034 19990101 20010101
4873860 1006821035 19990101 20020101
4873860 1006821054 19680101 19990101