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
124375612 12437561 2 F 20160805 20160606 20160810 EXP JP-009507513-1606JPN001734 MERCK 85.00 YR M Y 0.00000 20160810 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
124375612 12437561 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 50 MG, QD U 21995 50 MG TABLET QD
124375612 12437561 2 C TAKEPRON LANSOPRAZOLE 1 Oral 15 MG, QD U 0 15 MG TABLET QD
124375612 12437561 3 C MAGMITT MAGNESIUM OXIDE 1 Oral 330 MG, BID U 0 330 MG TABLET BID
124375612 12437561 4 C MICAMLO AMLODIPINE BESYLATETELMISARTAN 1 Oral 40 MG, QD U 0 40 MG TABLET QD
124375612 12437561 5 C ZYLORIC ALLOPURINOL 1 Oral 100 MG, QD U 0 100 MG TABLET QD
124375612 12437561 6 C AMITIZA LUBIPROSTONE 1 Oral 24 MICROGRAM, BID U 0 24 UG CAPSULE BID
124375612 12437561 7 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 Oral 60 MG, BID U 0 60 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124375612 12437561 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124375612 12437561 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124375612 12437561 Dizziness
124375612 12437561 Hypoglycaemia
124375612 12437561 Nausea

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
124375612 12437561 1 2014 0