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
106337492 10633749 2 F 20141027 20160628 20141205 20160705 EXP SE-JNJFOC-20141203120 JANSSEN 41.00 YR A M Y 0.00000 20160705 MD SE SE

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
106337492 10633749 1 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) STRENGTH: 100 MG Y N 103772 200 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106337492 10633749 1 Familial mediterranean fever

Outcome of event

Event ID CASEID OUTC COD
106337492 10633749 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106337492 10633749 Blood pressure decreased
106337492 10633749 Chills
106337492 10633749 Hypersensitivity
106337492 10633749 Infusion related reaction
106337492 10633749 Nausea
106337492 10633749 Off label use
106337492 10633749 Product use issue
106337492 10633749 Pyrexia
106337492 10633749 Vomiting

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
106337492 10633749 1 20141027 20141027 0