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
107479515 10747951 5 F 2011 20160905 20150129 20160908 EXP BR-JNJFOC-20150115470 JANSSEN 0.00 A M Y 0.00000 20160908 CN BR BR

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
107479515 10747951 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N UNKNOWN 0 LYOPHILIZED POWDER
107479515 10747951 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N UNKNOWN 0 LYOPHILIZED POWDER
107479515 10747951 3 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N UNKNOWN 103772 300 MG LYOPHILIZED POWDER
107479515 10747951 4 C CHLOROQUINE. CHLOROQUINE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107479515 10747951 1 Ankylosing spondylitis
107479515 10747951 2 Ankylosing spondylitis
107479515 10747951 3 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
107479515 10747951 HO
107479515 10747951 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107479515 10747951 Ankylosing spondylitis
107479515 10747951 Back injury
107479515 10747951 Blood pressure increased
107479515 10747951 Drug ineffective
107479515 10747951 Pain

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
107479515 10747951 1 20141016 0
107479515 10747951 2 20160709 0
107479515 10747951 3 200906 0