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
125609871 12560987 1 I 20160622 20160711 20160715 20160715 PER US-009507513-1607USA005068 MERCK 79.50 YR F Y 0.00000 20160715 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
125609871 12560987 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, DAILY Y Y 21995 100 MG FILM-COATED TABLET QD
125609871 12560987 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, DAILY Y Y 21995 100 MG FILM-COATED TABLET QD
125609871 12560987 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 U 0
125609871 12560987 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 U 0
125609871 12560987 5 C AMLODIPINE AMLODIPINE BESYLATE 1 U 0
125609871 12560987 6 C PREDNISONE. PREDNISONE 1 U 0 TABLET
125609871 12560987 7 C CRESTOR ROSUVASTATIN CALCIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125609871 12560987 1 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125609871 12560987 Arthralgia

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
125609871 12560987 1 20160621 201606 0
125609871 12560987 2 201606 20160701 0