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
109349223 10934922 3 F 20150209 20160810 20150320 20160816 EXP CO-ABBVIE-15K-036-1363610-00 ABBVIE 43.84 YR M Y 61.00000 KG 20160816 CN COUNTRY NOT SPECIFIED CO

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
109349223 10934922 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
109349223 10934922 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
109349223 10934922 3 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109349223 10934922 1 Ankylosing spondylitis
109349223 10934922 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
109349223 10934922 HO
109349223 10934922 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109349223 10934922 Arthralgia
109349223 10934922 Gait disturbance
109349223 10934922 Hip arthroplasty

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
109349223 10934922 1 20131121 20150714 0
109349223 10934922 2 201606 0