The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5659093 6522720 F 1 5659093-6 20070917 20071127 20080219 PER WAES 0709USA04050 MERCK + CO., INC. 84 YR M N 20080215 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5659093 1009627597 PS JANUVIA 1 ORAL 100 MG/DAILY/PO D D 21995
5659093 1010090773 C ATENOLOL 1
5659093 1010090774 C FELODIPINE 1
5659093 1010090775 C GLYBURIDE 1
5659093 1010090776 C METFORMIN HCL 1
5659093 1010090777 C PENTOXIFYLLINE 1
5659093 1010090778 C SIMVASTATIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5659093 1009627597 TYPE 2 DIABETES MELLITUS

Outcome of event

no results found

Reactions reported

Event ID PT
5659093 RASH MACULO-PAPULAR
5659093 RASH PRURITIC

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
5659093 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5659093 1009627597 20070801