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
125481492 12548149 2 F 20160823 20160712 20160907 PER US-009507513-1606USA008289 MERCK 0.00 F Y 104.31000 KG 20160907 MD 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
125481492 12548149 1 PS JANUMET XR METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 50/1000 MG, BID 22044 1 DF PROLONGED-RELEASE TABLET BID
125481492 12548149 2 C PRESERVISION AREDS 2 2 1 DF, BID U 0 1 DF BID
125481492 12548149 3 C CARVEDILOL. CARVEDILOL 1 3.125 MG, QD U 0 QD
125481492 12548149 4 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 20 MEQ, QD U 0 20 MEQ QD
125481492 12548149 5 C FUROSEMIDE. FUROSEMIDE 1 Oral 40 MG, QD U 0 40 MG TABLET QD
125481492 12548149 6 C ALLOPURINOL. ALLOPURINOL 1 300 MG, QD U 0 300 MG QD
125481492 12548149 7 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 20 MG, QD U 0 20 MG CAPSULE QD
125481492 12548149 8 C CELEBREX CELECOXIB 1 Oral 200 MG, QD U 0 200 MG CAPSULE QD
125481492 12548149 9 C ASPIRIN. ASPIRIN 1 81 MG, QD U 0 81 MG TABLET QD
125481492 12548149 10 C LOMOTIL (atropine sulfate (+) diphenoxylate hydrochloride) 2 2.5/0.025 MG ONCE DAILY, PRN U 0
125481492 12548149 11 C HUMALOG MIX 75/25 2 100 UNIT, 8CC INSULIN INJECTION U 0 INJECTION
125481492 12548149 12 C PRINIVIL LISINOPRIL 1 20 MG, QD U 0 20 MG TABLET QD
125481492 12548149 13 C SERTRALINE HYDROCHLORIDE. SERTRALINE HYDROCHLORIDE 1 100 MG, QD U 0 100 MG QD
125481492 12548149 14 C GABAPENTIN. GABAPENTIN 1 Oral 400 MG, TID U 0 400 MG TABLET TID
125481492 12548149 15 C COLESTIPOL HYDROCHLORIDE. COLESTIPOL HYDROCHLORIDE 1 Oral 1 TABLET, 3 TIMES DAILY, PRN U 0 TABLET
125481492 12548149 16 C KLOR-CON POTASSIUM CHLORIDE 1 Oral 1 DF, QD U 0 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125481492 12548149 1 Blood glucose increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125481492 12548149 Diarrhoea
125481492 12548149 Inappropriate schedule of drug administration

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

no results found

Therapies reported

no results found