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
127622701 12762270 1 I 20160910 20160920 20160920 EXP US-SA-2016SA169155 AVENTIS 0.00 A M Y 0.00000 20160920 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
127622701 12762270 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:140 UNIT(S) U UNK 21081 QD
127622701 12762270 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:70 UNIT(S) U UNK 21081 BID
127622701 12762270 3 C SOLOSTAR DEVICE 1 0 QD
127622701 12762270 4 C SOLOSTAR DEVICE 1 0 BID
127622701 12762270 5 C TOUJEO INSULIN GLARGINE 1 DOSE:70 UNIT(S) 0 BID
127622701 12762270 6 C SOLOSTAR DEVICE 1 0
127622701 12762270 7 C VICTOZA LIRAGLUTIDE 1 0
127622701 12762270 8 C JANUVIA SITAGLIPTIN PHOSPHATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127622701 12762270 1 Diabetes mellitus
127622701 12762270 2 Diabetes mellitus
127622701 12762270 3 Diabetes mellitus
127622701 12762270 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127622701 12762270 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127622701 12762270 Blood glucose increased
127622701 12762270 Fall
127622701 12762270 Hypoacusis
127622701 12762270 Joint injury
127622701 12762270 Off label use

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

no results found

Therapies reported

no results found