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
127587201 12758720 1 I 20160917 0 20160918 20160918 DIR US-FDA-350913 FDA-CTU 62.00 YR M N 76.50000 KG 20160918 N 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
127587201 12758720 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral Y Y MO34598 20160703 99 1 DF BID
127587201 12758720 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
127587201 12758720 5 C LANSOPRAZOLE DR 2 0
127587201 12758720 7 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 0
127587201 12758720 9 C RISPERIDONE. RISPERIDONE 1 0
127587201 12758720 11 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127587201 12758720 1 Blood glucose abnormal

Outcome of event

Event ID CASEID OUTC COD
127587201 12758720 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127587201 12758720 Gastric disorder
127587201 12758720 Headache
127587201 12758720 Nonspecific reaction
127587201 12758720 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
127587201 12758720 1 20160815 20160918 0