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
125671332 12567133 2 F 20140811 20160712 20160718 20160721 EXP IT-SA-2016SA128242 AVENTIS 73.00 YR E M Y 60.00000 KG 20160721 MD IT IT

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
125671332 12567133 1 PS INSULIN GLARGINE INSULIN GLARGINE 1 Subcutaneous UNKNOWN 21081 QD
125671332 12567133 2 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral Y UNKNOWN 0
125671332 12567133 3 C COUMADIN WARFARIN SODIUM 1 Oral 0 5 MG TABLET
125671332 12567133 4 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 0 75 MG FILM-COATED TABLET
125671332 12567133 5 C SIVASTIN SIMVASTATIN 1 Oral 0 40 MG FILM-COATED TABLET
125671332 12567133 6 C TAMSULOSIN HYDROCHLORIDE. TAMSULOSIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125671332 12567133 1 Type 2 diabetes mellitus
125671332 12567133 2 Type 2 diabetes mellitus
125671332 12567133 3 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125671332 12567133 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125671332 12567133 Hypoglycaemia
125671332 12567133 Loss of consciousness
125671332 12567133 Malaise
125671332 12567133 Presyncope

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

no results found

Therapies reported

no results found