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
125321811 12532181 1 I 20160602 20160701 20160706 20160706 EXP PH-009507513-1607PHL000916 MERCK 77.00 YR F Y 0.00000 20160706 CN PH PH

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
125321811 12532181 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 1 TABLET (50/500MG), QD 22044 1 DF FILM-COATED TABLET QD
125321811 12532181 2 C ATORVASTATIN ATORVASTATIN 1 UNK U 0
125321811 12532181 3 C TWYNSTA AMLODIPINE BESYLATETELMISARTAN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125321811 12532181 1 Diabetes mellitus
125321811 12532181 2 Blood cholesterol increased
125321811 12532181 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125321811 12532181 HO
125321811 12532181 DE
125321811 12532181 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125321811 12532181 Cardiac arrest
125321811 12532181 Inappropriate schedule of drug administration

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
125321811 12532181 1 2014 0
125321811 12532181 2 2012 0
125321811 12532181 3 2012 0