The Safety Rates Drug Report

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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
126131591 12613159 1 I 20160324 20160802 20160802 PER US-APOTEX-2016AP007516 APOTEX 47.00 YR F Y 99.80000 KG 20160802 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
126131591 12613159 1 PS GLIPIZIDE. GLIPIZIDE 1 Unknown 5 MG, EVERY MORNING AND EVENING 75795 5 MG TABLET BID
126131591 12613159 2 SS GLIPIZIDE. GLIPIZIDE 1 Unknown 10 MG, BID 75795 10 MG TABLET BID
126131591 12613159 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 500 MG, EVERY MORNING AND EVENING U U 0 500 MG BID
126131591 12613159 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 1000 MG, BID U U 0 1000 MG BID
126131591 12613159 5 C LISINOPRIL. LISINOPRIL 1 Unknown 10 MG, DAILY U U 0 10 MG
126131591 12613159 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown 25 MG DAILY U U 0 25 MG
126131591 12613159 7 C ATORVASTATIN ATORVASTATIN 1 Unknown 20 MG AT BEDTIME U U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126131591 12613159 1 Type 2 diabetes mellitus
126131591 12613159 3 Type 2 diabetes mellitus
126131591 12613159 5 Hypertension
126131591 12613159 6 Hypertension
126131591 12613159 7 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126131591 12613159 Hypoglycaemia
126131591 12613159 Treatment noncompliance
126131591 12613159 Weight increased

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

no results found

Therapies reported

no results found