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
106668053 10666805 3 F 201008 20160912 20141222 20160916 EXP FR-009507513-1101FRA00048 MERCK 77.00 YR F Y 0.00000 20160916 CN FR FR

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
106668053 10666805 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, QD Y 21995 100 MG FILM-COATED TABLET QD
106668053 10666805 2 C TAREG VALSARTAN 1 U 0
106668053 10666805 3 C CRESTOR ROSUVASTATIN CALCIUM 1 U 0
106668053 10666805 4 C BISOPROLOL BISOPROLOL 1 U 0
106668053 10666805 5 C FIXICAL CALCIUM CARBONATE 1 U 0
106668053 10666805 6 C ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 U 0
106668053 10666805 7 C KARDEGIC ASPIRIN LYSINE 1 U 0
106668053 10666805 8 C METFORMIN METFORMIN HYDROCHLORIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106668053 10666805 1 Type 2 diabetes mellitus
106668053 10666805 2 Hypertension
106668053 10666805 3 Hypertriglyceridaemia

Outcome of event

Event ID CASEID OUTC COD
106668053 10666805 OT
106668053 10666805 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106668053 10666805 Pemphigoid

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
106668053 10666805 1 20100604 201010 0