The Safety Rates Drug Report

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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
125884391 12588439 1 I 20160614 20160725 20160725 PER US-JNJFOC-20160617769 JANSSEN 0.00 A F Y 0.00000 20160725 PH 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
125884391 12588439 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 UNSPECIFIED
125884391 12588439 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 UNSPECIFIED
125884391 12588439 3 SS DIPHENHYDRAMINE HYDROCHLORIDE. DIPHENHYDRAMINE HYDROCHLORIDE 1 Unknown U U 999999 UNSPECIFIED
125884391 12588439 4 C REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 15MD05551 0 600 MG LYOPHILIZED POWDER
125884391 12588439 5 C REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 15MD05551 0 600 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125884391 12588439 2 Premedication
125884391 12588439 3 Premedication
125884391 12588439 4 Rheumatoid arthritis
125884391 12588439 5 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125884391 12588439 Off label use
125884391 12588439 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
125884391 12588439 4 20160614 0
125884391 12588439 5 2015 0