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
7386255 7861684 F 7386255-2 20110224 20110321 20110331 EXP US-NOVOPROD-324132 NOVOPROD 32 YR M Y 92.9 KG 20110331 MD 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
7386255 1016137015 SS NOVORAPID FLEXPEN 2 SUBCUTANEOUS 67 IU, QD 020986
7386255 1016137018 C CLONIDINE 1 0.1 MG, QD
7386255 1016137016 SS INSULATARD HM(GE) 2 SUBCUTANEOUS 50 IU, QD
7386255 1016137017 C BENADRYL 1 50 MG, UNK
7386255 1016137011 SS IDEG FLEXPEN 2 SUBCUTANEOUS 63 IU, QD
7386255 1016137012 SS IDEG FLEXPEN 2 SUBCUTANEOUS 63 IU, QD
7386255 1016137013 SS IDEG FLEXPEN 2 SUBCUTANEOUS 63 IU, QD
7386255 1016137014 PS NOVORAPID FLEXPEN 2 SUBCUTANEOUS 67 IU, QD 020986
7386255 1016137019 C ALTACE 1 ORAL 2.5 MG, QD

Indications of drugs used

Event ID DRUG SEQ INDI PT
7386255 1016137018 HYPERTENSION
7386255 1016137016 TYPE 1 DIABETES MELLITUS
7386255 1016137011 TYPE 1 DIABETES MELLITUS
7386255 1016137014 TYPE 1 DIABETES MELLITUS
7386255 1016137019 HYPERTENSION

Outcome of event

Event ID OUTC COD
7386255 HO

Reactions reported

Event ID PT
7386255 DIABETIC KETOACIDOSIS
7386255 HYPOVOLAEMIA
7386255 HYPEROSMOLAR STATE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7386255 1016137015 20110226
7386255 1016137018 20100925
7386255 1016137016 20100930 20101006 6 DAY
7386255 1016137017 20110224
7386255 1016137011 20100401 20100929 181 DAY
7386255 1016137012 20101007 20110224 140 DAY
7386255 1016137013 20110228
7386255 1016137014 20100401 20110224 329 DAY
7386255 1016137019 20090101