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
126860381 12686038 1 I 20160226 20160825 20160825 PER US-NOVOPROD-483323 NOVO NORDISK 62.00 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
126860381 12686038 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD ES6T412 22341 .6 MG SOLUTION FOR INJECTION QD
126860381 12686038 2 SS BUPROPION. BUPROPION 1 Oral 100 MG, UNK UNKNOWN 0 100 MG
126860381 12686038 3 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 30 MG, UNK UNKNOWN 0 30 MG
126860381 12686038 4 SS ESTRACE ESTRADIOL 1 Oral 0.5 MG, UNK UNKNOWN 0 .5 MG
126860381 12686038 5 SS LOSARTAN. LOSARTAN 1 Oral 100 MG, UNK UNKNOWN 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126860381 12686038 1 Type 2 diabetes mellitus
126860381 12686038 2 Pain
126860381 12686038 3 Gastrooesophageal reflux disease
126860381 12686038 4 Product used for unknown indication
126860381 12686038 5 Blood pressure increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126860381 12686038 Blood glucose increased
126860381 12686038 Blood pressure increased
126860381 12686038 Diarrhoea
126860381 12686038 Headache
126860381 12686038 Muscle spasms

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
126860381 12686038 1 20160204 0