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
125469391 12546939 1 I 20160603 20160627 20160711 20160711 EXP PT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-055566 BRISTOL MYERS SQUIBB 81.52 YR F Y 0.00000 20160711 CN PT PT

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
125469391 12546939 1 PS RISIDON METFORMIN HYDROCHLORIDE 1 Oral 2000 MG, QD Y 20357 2000 MG QD
125469391 12546939 2 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 1 DF, BID Y 0 1 DF TABLET BID
125469391 12546939 3 C EPINITRIL NITROGLYCERIN 1 Transdermal U 0 TRANSDERMAL PATCH
125469391 12546939 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 1 DF, QD U 0 1 DF QD
125469391 12546939 5 C IRBESARTAN. IRBESARTAN 1 Unknown 1 DF, QD U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125469391 12546939 1 Type 2 diabetes mellitus
125469391 12546939 2 Type 2 diabetes mellitus
125469391 12546939 3 Product used for unknown indication
125469391 12546939 4 Product used for unknown indication
125469391 12546939 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125469391 12546939 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125469391 12546939 Blood creatinine increased
125469391 12546939 Dehydration
125469391 12546939 Diarrhoea
125469391 12546939 Metabolic acidosis

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
125469391 12546939 1 20160610 0
125469391 12546939 2 20160610 0