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
124867203 12486720 3 F 20160912 20160621 20160916 EXP US-009507513-1606USA003819 MERCK 66.00 YR F Y 101.59000 KG 20160916 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
124867203 12486720 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral UNK U 22044 FILM-COATED TABLET
124867203 12486720 2 SS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral UNK U 22044 FILM-COATED TABLET
124867203 12486720 3 SS METFORMIN METFORMIN HYDROCHLORIDE 1 UNK N 0
124867203 12486720 4 C GLIPIZIDE. GLIPIZIDE 1 10 MG, TWICE A DAY, ONE IN THE MORNING AND ONE IN THE NIGHT U 0 10 MG BID
124867203 12486720 5 C HYDROCODONE HYDROCODONE 1 10/325 U 0
124867203 12486720 6 C GABAPENTIN. GABAPENTIN 1 U 0
124867203 12486720 7 C CLARITIN LORATADINE 1 THREE TIMES A MONTH U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124867203 12486720 1 Type 2 diabetes mellitus
124867203 12486720 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124867203 12486720 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124867203 12486720 Abdominal pain upper
124867203 12486720 Asthenia
124867203 12486720 Constipation
124867203 12486720 Diarrhoea
124867203 12486720 Malaise
124867203 12486720 Peripheral swelling

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
124867203 12486720 1 201604 0
124867203 12486720 2 2016 0
124867203 12486720 3 201604 2016 0