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
124913132 12491313 2 F 20160816 20160816 20160623 20160829 PER US-AMGEN-USASP2016077795 AMGEN 20.00 YR A F Y 0.00000 20160829 MD 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
124913132 12491313 1 PS ENBREL ETANERCEPT 1 Unknown UNK 1064425 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
124913132 12491313 2 SS HUMIRA ADALIMUMAB 1 Unknown UNK 0
124913132 12491313 3 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
124913132 12491313 4 SS OTEZLA APREMILAST 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124913132 12491313 1 Juvenile idiopathic arthritis
124913132 12491313 2 Product used for unknown indication
124913132 12491313 3 Product used for unknown indication
124913132 12491313 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124913132 12491313 Drug dose omission
124913132 12491313 Drug effect decreased
124913132 12491313 Drug ineffective
124913132 12491313 Headache
124913132 12491313 Injection site haemorrhage
124913132 12491313 Injection site pain
124913132 12491313 Malaise
124913132 12491313 Underdose
124913132 12491313 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found