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
106645183 10664518 3 F 201008 20160912 20141219 20160916 EXP FR-009507513-1102FRA00105 MERCK 79.00 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
106645183 10664518 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, QD Y 21995 100 MG FILM-COATED TABLET QD
106645183 10664518 2 C OROCAL D3 CALCIUM CARBONATECHOLECALCIFEROL 1 Oral U 0 TABLET
106645183 10664518 3 C DIFFU-K POTASSIUM CHLORIDE 1 Oral 0 TABLET
106645183 10664518 4 C KERLONE BETAXOLOL HYDROCHLORIDE 1 Oral UNK MG, UNK 0 TABLET
106645183 10664518 5 C ESIDREX HYDROCHLOROTHIAZIDE 1 Oral UNK MG, UNK 0 TABLET
106645183 10664518 6 C LANSOPRAZOLE. LANSOPRAZOLE 1 Oral UNK MG, UNK 0 TABLET
106645183 10664518 7 C ARESTAL LOPERAMIDE OXIDE 1 Oral 0 TABLET
106645183 10664518 8 C ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Oral 0 TABLET
106645183 10664518 9 C LIORAM 2 Oral 0 TABLET
106645183 10664518 10 C ELISOR PRAVASTATIN SODIUM 1 Oral UNK MG, UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106645183 10664518 1 Type 2 diabetes mellitus
106645183 10664518 4 Hypertension
106645183 10664518 5 Hypertension
106645183 10664518 6 Gastrooesophageal reflux disease
106645183 10664518 10 Dyslipidaemia

Outcome of event

Event ID CASEID OUTC COD
106645183 10664518 HO
106645183 10664518 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106645183 10664518 Pemphigoid
106645183 10664518 Pruritus
106645183 10664518 Urticaria

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
106645183 10664518 1 20100709 20110124 0