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
125888561 12588856 1 I 2016 20160617 20160725 20160725 PER US-JNJFOC-20160618816 JANSSEN 6.00 DEC A F Y 0.00000 20160725 OT 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
125888561 12588856 1 PS TYLENOL ACETAMINOPHEN 1 Unknown U U 19872 UNSPECIFIED
125888561 12588856 2 SS TYLENOL ACETAMINOPHEN 1 Unknown U U 19872 UNSPECIFIED
125888561 12588856 3 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral U U 999999 25 MG UNSPECIFIED
125888561 12588856 4 C REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 0 500 MG SOLUTION FOR INJECTION
125888561 12588856 5 C REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 0 300 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125888561 12588856 2 Premedication
125888561 12588856 3 Premedication
125888561 12588856 4 Rheumatoid arthritis
125888561 12588856 5 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125888561 12588856 Off label use
125888561 12588856 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
125888561 12588856 2 2016 0
125888561 12588856 3 2016 0
125888561 12588856 4 2016 2016 0
125888561 12588856 5 2016 0