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
98126505 9812650 5 F 2014 20160704 20140113 20160718 EXP BR-JNJFOC-20140103761 JANSSEN 0.00 A M Y 87.00000 KG 20160718 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
98126505 9812650 1 SS SIMPONI GOLIMUMAB 1 Subcutaneous 1 MONTH INTERVAL U UNSPECIFIED;UNSPECIFIED +MORE 0 SOLUTION FOR INJECTION
98126505 9812650 2 PS SIMPONI GOLIMUMAB 1 Subcutaneous U UNSPECIFIED;UNSPECIFIED +MORE 125289 SOLUTION FOR INJECTION
98126505 9812650 3 SS ENBREL ETANERCEPT 1 Unknown U 0 UNSPECIFIED
98126505 9812650 4 SS HUMIRA ADALIMUMAB 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98126505 9812650 1 Ankylosing spondylitis
98126505 9812650 2 Ankylosing spondylitis
98126505 9812650 3 Product used for unknown indication
98126505 9812650 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
98126505 9812650 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98126505 9812650 Adverse event
98126505 9812650 Drug ineffective
98126505 9812650 Glucose tolerance impaired

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
98126505 9812650 1 20150201 20151001 0
98126505 9812650 2 2014 2014 0