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
125822641 12582264 1 I 0 20160721 20160721 DIR 0.00 F N 0.00000 20160720 N 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
125822641 12582264 1 PS LANTUS INSULIN GLARGINE 1 0
125822641 12582264 2 SS NOVOLIN INSULIN HUMAN 1 0
125822641 12582264 3 SS NOVOLOG INSULIN ASPART 1 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125822641 12582264 Blood cholesterol increased
125822641 12582264 Blood glucose increased
125822641 12582264 Burning sensation
125822641 12582264 Glycosylated haemoglobin increased
125822641 12582264 Injection site pain
125822641 12582264 Muscle spasms
125822641 12582264 Pain

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

no results found

Therapies reported

no results found