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
102775315 10277531 5 F 2012 20160719 20140703 20160727 EXP CA-ABBVIE-14K-028-1254081-00 ABBVIE 0.00 M Y 73.55000 KG 20160727 MD COUNTRY NOT SPECIFIED 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
102775315 10277531 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102775315 10277531 1 Ankylosing spondylitis

Outcome of event

Event ID CASEID OUTC COD
102775315 10277531 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102775315 10277531 Ankylosing spondylitis
102775315 10277531 Arthralgia
102775315 10277531 Dizziness
102775315 10277531 Drug ineffective
102775315 10277531 Dysphagia
102775315 10277531 Dyspnoea
102775315 10277531 Fatigue
102775315 10277531 Feeling abnormal
102775315 10277531 Gait disturbance
102775315 10277531 Inappropriate schedule of drug administration
102775315 10277531 Insomnia
102775315 10277531 Joint swelling
102775315 10277531 Lipohypertrophy
102775315 10277531 Loss of consciousness
102775315 10277531 Mobility decreased
102775315 10277531 Nuchal rigidity
102775315 10277531 Pain
102775315 10277531 Palpitations
102775315 10277531 Panic attack
102775315 10277531 Respiratory disorder
102775315 10277531 Tooth loss
102775315 10277531 Unevaluable event

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
102775315 10277531 1 20070301 0