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
77277812 7727781 2 F 201001 20160624 20101222 20160707 EXP US-SANOFI-AVENTIS-2010SA075888 AVENTIS 59.00 YR A F Y 121.00000 KG 20160707 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
77277812 7727781 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous 73 TO 77 UNITS Y U 0F525A 21081 SOLUTION FOR INJECTION QD
77277812 7727781 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE:65 UNIT(S) Y U UNKNOWN 21081 SOLUTION FOR INJECTION QD
77277812 7727781 3 C SOLOSTAR DEVICE 1 0F525A 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77277812 7727781 1 Type 2 diabetes mellitus
77277812 7727781 2 Type 2 diabetes mellitus
77277812 7727781 3 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
77277812 7727781 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
77277812 7727781 Arthritis
77277812 7727781 Back disorder
77277812 7727781 Blood glucose decreased
77277812 7727781 Breast cancer
77277812 7727781 Decreased appetite
77277812 7727781 Myalgia
77277812 7727781 Tremor
77277812 7727781 Weight decreased

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
77277812 7727781 1 2010 0
77277812 7727781 3 2010 0