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
94836964 9483696 4 F 20110208 20160714 20130828 20160719 EXP CA-JNJFOC-20130815052 JANSSEN 50.46 YR A M Y 138.00000 KG 20160719 CN CA CA

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
94836964 9483696 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 650 MG LYOPHILIZED POWDER
94836964 9483696 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 103772 650 MG LYOPHILIZED POWDER
94836964 9483696 3 C JENTADUETO LINAGLIPTINMETFORMIN HYDROCHLORIDE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94836964 9483696 1 Crohn's disease
94836964 9483696 2 Crohn's disease
94836964 9483696 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
94836964 9483696 HO
94836964 9483696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
94836964 9483696 Herpes zoster
94836964 9483696 Kidney infection
94836964 9483696 Nephrolithiasis
94836964 9483696 Off label use
94836964 9483696 Product use issue

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
94836964 9483696 1 20160603 0
94836964 9483696 2 20110208 0