PURPOSE OF REVIEW: Due to continuous development of new drugs and better treatment strategies, survival of patients with cystic fibrosis has changed dramatically. Recently, targeted therapy of cystic fibrosis transmembrane conductance regulator (CFTR) modulators have become available. Despite these promising developments, treatment of this complex multiorgan disease constitutes a high and variable amount of other drugs. Complications of pharmacotherapeutic treatment are, therefore, expected to become more prevalent. This gives cause to review drug-related side effects in this new era in cystic fibrosis treatment. RECENT FINDINGS: We will discuss cystic fibrosis-related pharmacotherapies with a focus on indication of treatment, side effects ...
Abstract Objectives Study of currently approved drugs and exploration of future clinical development...
Purpose of review Several new therapeutic modalities have recently become available to be used in pa...
Cystic fibrosis is an autosomal recessive genetic disorder, characterized by mutation in the cystic ...
PURPOSE OF REVIEW: Due to continuous development of new drugs and better treatment strategies, survi...
Introduction: Cystic fibrosis (CF) is a lung disease that involves more than 80,000 people globally....
Cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies target the underlying...
This review seeks to re-introduce cystic fibrosis (CF) clinicians to the pharmacology of drug-drug i...
Azithromycin has antimicrobial, immunomodulatory, and anti-inflammatory effects for chronic inflamm...
Introduction: Cystic fibrosis (CF) is a genetic disease affecting multiple organ systems. Research a...
Purpose of review This review will discuss the challenges of defining a pulmonary exacerbations in c...
ABSTRACT: During what is a relatively barren time for new therapies for cystic fibrosis (CF), azithr...
Cystic fibrosis (CF) is one of the commonest life-limiting genetic disorders in the Caucasian popula...
Purpose of review : The introduction of highly effective cystic fibrosis transmembrane conduc...
Cystic fibrosis (CF) is a reversed autosomal genetic disease that originates from some white or cauc...
Cystic fibrosis is the most common life-threatening recessively inherited disease in Caucasians. Due...
Abstract Objectives Study of currently approved drugs and exploration of future clinical development...
Purpose of review Several new therapeutic modalities have recently become available to be used in pa...
Cystic fibrosis is an autosomal recessive genetic disorder, characterized by mutation in the cystic ...
PURPOSE OF REVIEW: Due to continuous development of new drugs and better treatment strategies, survi...
Introduction: Cystic fibrosis (CF) is a lung disease that involves more than 80,000 people globally....
Cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies target the underlying...
This review seeks to re-introduce cystic fibrosis (CF) clinicians to the pharmacology of drug-drug i...
Azithromycin has antimicrobial, immunomodulatory, and anti-inflammatory effects for chronic inflamm...
Introduction: Cystic fibrosis (CF) is a genetic disease affecting multiple organ systems. Research a...
Purpose of review This review will discuss the challenges of defining a pulmonary exacerbations in c...
ABSTRACT: During what is a relatively barren time for new therapies for cystic fibrosis (CF), azithr...
Cystic fibrosis (CF) is one of the commonest life-limiting genetic disorders in the Caucasian popula...
Purpose of review : The introduction of highly effective cystic fibrosis transmembrane conduc...
Cystic fibrosis (CF) is a reversed autosomal genetic disease that originates from some white or cauc...
Cystic fibrosis is the most common life-threatening recessively inherited disease in Caucasians. Due...
Abstract Objectives Study of currently approved drugs and exploration of future clinical development...
Purpose of review Several new therapeutic modalities have recently become available to be used in pa...
Cystic fibrosis is an autosomal recessive genetic disorder, characterized by mutation in the cystic ...