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
126860731 12686073 1 I 20160216 20160229 20160825 20160825 PER US-NOVOPROD-483518 NOVO NORDISK 0.00 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
126860731 12686073 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous U U UNKNOWN 22341 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126860731 12686073 1 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126860731 12686073 Abdominal pain
126860731 12686073 Asthenia
126860731 12686073 Blood glucose abnormal
126860731 12686073 Blood glucose decreased
126860731 12686073 Dyspnoea
126860731 12686073 Feeling abnormal
126860731 12686073 Feeling jittery
126860731 12686073 Flushing
126860731 12686073 Functional gastrointestinal disorder
126860731 12686073 Headache
126860731 12686073 Hyperhidrosis
126860731 12686073 Incorrect dose administered by device
126860731 12686073 Nausea
126860731 12686073 Palpitations
126860731 12686073 Paraesthesia

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

no results found

Therapies reported

no results found