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
116434152 11643415 2 F 20150921 20160826 20151020 20160830 EXP CO-ABBVIE-15K-036-1483940-00 ABBVIE 61.37 YR F Y 68.00000 KG 20160830 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
116434152 11643415 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
116434152 11643415 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116434152 11643415 1 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
116434152 11643415 HO
116434152 11643415 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116434152 11643415 Contusion
116434152 11643415 Fall
116434152 11643415 Forearm fracture
116434152 11643415 Laceration
116434152 11643415 Mobility decreased
116434152 11643415 Post-traumatic pain

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
116434152 11643415 1 20120808 20150909 0