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
124030554 12403055 4 F 20160519 20160722 20160525 20160728 EXP JP-009507513-1605JPN010970 MERCK 64.00 YR M Y 59.00000 KG 20160728 PH JP JP

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
124030554 12403055 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 50 MG, QD 21995 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124030554 12403055 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124030554 12403055 HO
124030554 12403055 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124030554 12403055 Altered state of consciousness
124030554 12403055 Drug dose omission
124030554 12403055 Hepatitis alcoholic
124030554 12403055 Hypoglycaemia

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
124030554 12403055 1 20160501 0