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
125568551 12556855 1 I 2008 20160418 20160714 20160714 PER US-SA-2016SA078735 AVENTIS 0.00 F Y 0.00000 20160714 OT 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
125568551 12556855 1 PS GLIMEPIRIDE. GLIMEPIRIDE 1 Unknown U UNK 20496 10 MG QD
125568551 12556855 2 SS GLIPIZIDE. GLIPIZIDE 1 Unknown U UNK 0 10 MG QD
125568551 12556855 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125568551 12556855 1 Type 2 diabetes mellitus
125568551 12556855 2 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125568551 12556855 Blood glucose increased
125568551 12556855 Rash
125568551 12556855 Urticaria

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
125568551 12556855 1 201510 201511 0
125568551 12556855 2 201601 20160407 0