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
126856471 12685647 1 I 20150805 20150807 20160825 20160825 PER US-NOVOPROD-461002 NOVO NORDISK 54.00 YR A F Y 0.00000 20160825 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
126856471 12685647 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD 1.3329999 MG Y U UNKNOWN 22341 .6 MG SOLUTION FOR INJECTION QD
126856471 12685647 2 C LANTUS INSULIN GLARGINE 1 Subcutaneous UNKNOWN 0
126856471 12685647 3 C ALEVE NAPROXEN SODIUM 1 0
126856471 12685647 4 C HUMIRA ADALIMUMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126856471 12685647 1 Type 2 diabetes mellitus
126856471 12685647 2 Type 2 diabetes mellitus
126856471 12685647 3 Arthritis
126856471 12685647 4 Arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126856471 12685647 Chills
126856471 12685647 Dysphagia
126856471 12685647 Headache
126856471 12685647 Nausea
126856471 12685647 Throat tightness
126856471 12685647 Tremor
126856471 12685647 Vertigo

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
126856471 12685647 1 20150803 20150806 0