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
123728673 12372867 3 F 20160704 20160516 20160706 EXP US-009507513-1605USA007702 MERCK 77.00 YR F Y 91.16000 KG 20160706 CN 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
123728673 12372867 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100MG N U L005591 21995 1 DF FILM-COATED TABLET
123728673 12372867 2 C PROVENTIL ALBUTEROL 1 U 0 INHALATION POWDER
123728673 12372867 3 C CLOTRIMAZOLE. CLOTRIMAZOLE 1 U 0
123728673 12372867 4 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 U 0 TABLET
123728673 12372867 5 C OXYGEN. OXYGEN 1 U 0
123728673 12372867 6 C ZOCOR SIMVASTATIN 1 U 0 TABLET
123728673 12372867 7 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 U 0
123728673 12372867 8 C PYRIDOXINE PYRIDOXINE 1 U 0
123728673 12372867 9 C CHOLECALCIFEROL CHOLECALCIFEROL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123728673 12372867 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
123728673 12372867 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123728673 12372867 Decreased appetite
123728673 12372867 Diarrhoea
123728673 12372867 Dizziness
123728673 12372867 Weight decreased

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
123728673 12372867 1 20130318 20150601 0