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
126307151 12630715 1 I 20160211 20160728 20160808 20160808 EXP RS-SA-2016SA139178 AVENTIS 81.00 YR E M Y 85.30000 KG 20160808 MD RS RS

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
126307151 12630715 1 PS AMARYL GLIMEPIRIDE 1 Unknown U UNKNOWN 20496
126307151 12630715 2 SS GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 Unknown U UNKNOWN 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126307151 12630715 HO
126307151 12630715 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126307151 12630715 Atrial fibrillation
126307151 12630715 Hypoglycaemia

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

no results found

Therapies reported

no results found