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
124015884 12401588 4 F 20160515 20160818 20160525 20160823 EXP US-009507513-1605USA011239 MERCK 77.57 YR F Y 59.86000 KG 20160823 OT 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
124015884 12401588 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 50 MG, DAILY 300 MG Y 21995 50 MG FILM-COATED TABLET QD
124015884 12401588 2 C METOPROLOL. METOPROLOL 1 UNK U 0
124015884 12401588 3 C COZAAR LOSARTAN POTASSIUM 1 Oral UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124015884 12401588 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124015884 12401588 HO
124015884 12401588 LT
124015884 12401588 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124015884 12401588 Diplopia
124015884 12401588 Disturbance in attention
124015884 12401588 Headache
124015884 12401588 Hypertensive crisis
124015884 12401588 Visual impairment
124015884 12401588 Vomiting

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
124015884 12401588 1 20160513 20160518 0