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
125738411 12573841 1 I 201506 20151013 20160720 20160720 EXP CA-PFIZER INC-2015345355 PFIZER 59.00 YR F Y 0.00000 20160720 CN CA CA

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
125738411 12573841 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK 0
125738411 12573841 2 SS ENBREL ETANERCEPT 1 UNK 0
125738411 12573841 3 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK 11719
125738411 12573841 4 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK 0
125738411 12573841 5 SS SIMPONI GOLIMUMAB 1 Subcutaneous UNK 0
125738411 12573841 6 SS STELARA USTEKINUMAB 1 Subcutaneous UNK 0
125738411 12573841 7 SS OTEZLA APREMILAST 1 UNK 0 TABLET
125738411 12573841 8 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125738411 12573841 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125738411 12573841 Drug effect decreased
125738411 12573841 Drug ineffective
125738411 12573841 Hypoaesthesia
125738411 12573841 Malaise
125738411 12573841 Mobility decreased
125738411 12573841 Rheumatoid arthritis

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

no results found

Therapies reported

no results found