Infliximab
Hypesrentitivity infusion reactions are common (PMID 12818276). For those ILD cases exposed to methotrexate concomitantly, drug causality assessment in regards to infliximab is difficult.
Hypesrentitivity infusion reactions are common (PMID 12818276). For those ILD cases exposed to methotrexate concomitantly, drug causality assessment in regards to infliximab is difficult.
Frequency - Incidence
Incidence of respiratory adverse event(s) due to the specific drug as assessed by number of reported/published cases in the literature. Red digits in stars indicate: 0 = Very rare, questionable signal · 1 = < 10 cases · 2 = 10-50 cases · 3 = 50–100 cases · 4 = 100-200 cases · 5 = >200 cases
Evidence level/grade
Evidence level for respiratory adverse event(s) due to the specific drug as estimated using Hill’s (1965), Naranjo’s (1981), and Bégaud’s (1985) criteria applied to published cases. Blue digits in stars indicate: 0 = Questionable · 1 = Low · 2 = Moderate · 3 = Robust · 4 = Definite · 5 = Unquestionable, pathognomonic
Pneumonitis (interstitial lung disease/ILD)
Pneumonitis (ILD), acute and/or severe (may cause ARDS)
Eosinophilic pneumonia (pulmonary infiltrates and eosinophilia)
Acute eosinophilic pneumonia (AEP)
Organizing pneumonia pattern (an area or areas of consolidation on imaging)
Pulmonary fibrosis
Rapidly progressive ILD/pulmonary fibrosis (Hamman-Rich syndrome)
Progression, acceleration or exacerbation of preexisting ILD/fibrosis
DRES syndrome - DRESS-like reaction
Antiphospholipid antibodies w/wo the APL syndrome
Lupus - Lupus syndrome (see also Vd)
Autoimmunity-Autoimmune conditions (+ANA, +anti-ds-DNA, +ANCAs, other auto-Abs)
Anaphylaxis-Anaphylactoid reaction (can be fatal)
Hypersensitivity reaction (may manifest with fever and/or skin, throat or airway involvement)
Eosinophilic granulomatosis with polyangiitis (Churg-Strauss)
Myopathy-Myositis-Polymyositis (see also under Xba)
Sarcoid-like granulomatosis (endo-/extrathoracic)
Vasculitis, pulmonary (w/wo AH), extrapulmonary, systemic: ANCA-positive
Granulomatosis with polyangiitis (typically ANCA pos.) - GPA flare
Relapse/flare/onset of Crohn's disease
Opportunistic pulmonary/systemic infections
Aspergillosis, pulmonary (invasive, allergic [ABPA], or mycetoma)
Pneumocystis jiroveci pulmonary colonization
Pneumocystis jiroveci pneumonia
Tuberculosis, miliary
Tuberculosis (pulmonary, pulmonary, extrapulmonary or disseminated). Reactivation or de novo
Nontuberculous pulmonary mycobacterial infection/superinfection
Legionella pneumophila pneumonia
Nocardia pulmonary/systemic infection
Viral pneumonia
Fungal infection (pulmonary/extrapulmonary)
Cryptococcus pulmonary and/or systemic infection
Histoplamosis (reactivation)
Actinomycosis