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
125713141 12571314 1 I 2009 20160711 20160719 20160719 EXP US-SA-2016SA128910 AVENTIS 64.00 YR A F Y 94.34000 KG 20160719 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
125713141 12571314 1 PS LANTUS INSULIN GLARGINE 1 Unknown U UNKNOWN 21081
125713141 12571314 2 C SIMVASTATIN. SIMVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125713141 12571314 2 Blood triglycerides abnormal

Outcome of event

Event ID CASEID OUTC COD
125713141 12571314 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125713141 12571314 Blood glucose increased
125713141 12571314 Glycosylated haemoglobin increased
125713141 12571314 Hypoaesthesia
125713141 12571314 Infection
125713141 12571314 Neuropathy peripheral
125713141 12571314 Renal disorder
125713141 12571314 Thyroid disorder
125713141 12571314 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
125713141 12571314 1 2009 2010 0