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
120543253 12054325 3 F 201506 20160629 20160209 20160707 EXP BR-JNJFOC-20160205704 JANSSEN 40.55 YR A F Y 0.00000 20160707 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
120543253 12054325 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) LAST INFUSION Y U UNKNOWN 0 LYOPHILIZED POWDER
120543253 12054325 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) Y U UNKNOWN 103772 LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120543253 12054325 1 Rheumatoid arthritis
120543253 12054325 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
120543253 12054325 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120543253 12054325 Arthralgia
120543253 12054325 Chondropathy
120543253 12054325 Dental caries
120543253 12054325 Dysstasia
120543253 12054325 Mouth injury
120543253 12054325 Mouth swelling
120543253 12054325 Pain in extremity
120543253 12054325 Toothache

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
120543253 12054325 1 20150611 0
120543253 12054325 2 20141110 0