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
126938172 12693817 2 F 20160912 20160829 20160922 PER US-009507513-1608USA011732 MERCK 0.00 M Y 0.00000 20160922 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
126938172 12693817 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral UNK D 22044 FILM-COATED TABLET
126938172 12693817 2 SS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral UNK D 22044 FILM-COATED TABLET
126938172 12693817 3 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126938172 12693817 1 Type 2 diabetes mellitus
126938172 12693817 3 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126938172 12693817 Asthenia
126938172 12693817 Diarrhoea
126938172 12693817 Malaise

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
126938172 12693817 1 201604 0
126938172 12693817 2 2016 0
126938172 12693817 3 201604 0