Last reviewed · How we verify

Theophylline Anhydrous Oral Tablet

Damanhour Teaching Hospital · FDA-approved active Small molecule

Theophylline is a nonselective phosphodiesterase inhibitor that increases intracellular cAMP and cGMP, producing bronchodilation and anti-inflammatory effects.

Theophylline is a nonselective phosphodiesterase inhibitor that increases intracellular cAMP and cGMP, producing bronchodilation and anti-inflammatory effects. Used for Asthma (chronic maintenance therapy), Chronic obstructive pulmonary disease (COPD), Apnea of prematurity.

At a glance

Generic nameTheophylline Anhydrous Oral Tablet
Also known asQuibron-T/SR tablets
SponsorDamanhour Teaching Hospital
Drug classNonselective phosphodiesterase inhibitor; xanthine derivative
TargetPhosphodiesterase enzymes (nonselective); adenosine receptors (antagonist)
ModalitySmall molecule
Therapeutic areaRespiratory/Pulmonology
PhaseFDA-approved

Mechanism of action

Theophylline works primarily by inhibiting phosphodiesterase enzymes, which prevents the breakdown of cyclic nucleotides (cAMP and cGMP) in smooth muscle and immune cells. This leads to relaxation of bronchial smooth muscle, resulting in bronchodilation. Additionally, theophylline has immunomodulatory properties including reduced inflammatory mediator release from mast cells and eosinophils, and enhanced diaphragmatic contractility.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: