Classes
DEA Class; Rx
Common Brand Names; Theo 24, Theochron, Elixophyllin, aminophylline, Uniphyl
- Xanthine Derivatives;
- Phosphodiesterase Enzyme Inhibitors, Nonselective
Description
Oral and intravenous methylxanthine
Used primarily for maintenance treatment of COPD or asthma but is not a preferred agent in either disease; also used in apnea of prematurity not responding to other therapies
Aminophylline is converted to theophylline systemically; 1 mg aminophylline = 0.8 mg theophylline
Indications
Indicated for the treatment of asthma exacerbation or for asthma maintenance treatment; or for maintenance treatment or exacerbations due to chronic obstructive pulmonary disease (COPD) (e.g., emphysema or chronic bronchitis).
Contraindications
Hypersensitivity
Adverse Effects
Peak serum concentration <20 mcg/mL
- Central nervous system excitement, headache, insomnia, irritability, restlessness, seizure
- Diarrhea, nausea, vomiting
- Diuresis (transient)
- Exfoliative dermatitis
- Skeletal muscle tremors
- Tachycardia, flutter
- Hypercalcemia (with concomitant hyperthyroid disease)
- Difficulty urinating (elderly males with prostatism)
Peak serum concentration >30 mcg/mL
- Acute myocardial infarction
- Seizures (resistant to anticonvulsants)
- Urinary retention
Warnings
Patients, who develop CNS abnormalities, reported (rarely) to experience nonconvulsive status epilepticus
Theophylline clearance may decrease in patients with congestive heart failure, acute pulmonary edema, hepatic disease, cor pulmonale, acute hepatitis, hypothyroidism, cirrhosis, fever, or sepsis with multiorgan failure and shock; severe and potentially fatal toxicity may occur if reduced theophylling clearance occurs
Avoid extravasation; vesicant; ensure proper placement of catherer prior to and during infusion
Use with caution in patients with hyperthyroidism, seizure disorder, peptic ulcer, or cardiovascular disease
Some dosage forms may contain propylene glycol; use caution; seizures, hyperosmolality, lactic acidosis, and respiratory depression reported associated with use of large amounts of propylene glycol
Measure serum levels and withhold subsequent doses if patient develops signs and symptoms of theophylline toxicity
Use caution in patients with cardiac arrhythmia, excluding bradyarrhythmia; use may exacerbate arrhythmia
Use with caution in patients with cystic fibrosis; increased theophylline clearance may occur
Use with caution in patients with seizure disorders; use may exacerbate seizure disorder
Do not increase dose in response to acute exacerbation of symptoms unless steady state serum theophylline concentration of <10 mcg//mL
Pregnancy and Lactation
Pregnancy category: C
Lactation: Theophylline is excreted into breast milk and may cause irritability or other signs of mild toxicity in nursing human infants; serious adverse effects in infant are unlikely unless mother has toxic serum theophylline concentration
Maximum Dosage
Theophylline has a narrow therapeutic index. The maximum dosage is individualized based on therapeutic drug concentration monitoring and assessment of efficacy and safety parameters. The following are some general guidelines in chronic use (dosage expressed as theophylline):
18 to 60 years: Adults requiring more than 600 mg/day total of theophylline require close monitoring to individualize dosage. It is recommended not to exceed 400 mg/day PO in patients with risk factors for decreased clearance or in whom recommended serum concentration monitoring is not possible.
60 years and older: Do not exceed 400 mg/day PO, as reduced clearance of theophylline is expected.
400 mg/day PO.
16 to 17 years: Individualize dosage; 400 mg/day PO, if risk factors for decreased clearance are present or recommended serum concentration monitoring is not possible.
13 to 15 years: Individualize dosage; 16 mg/kg/day up to 400 mg/day PO, if risk factors for decreased clearance are present or recommended serum concentration monitoring is not possible.
Individualize dosage; do not exceed 16 mg/kg/day up to 400 mg/day PO if risk factors for decreased clearance are present or recommended serum theophylline concentration monitoring is not possible.
Individualize dosage; infant dosing is based on age/weight.
Individualize dosage; loading doses of 8 mg/kg IV or PO have been used.
How supplied
Theophylline anhydrous
capsule, extended-release (24 hours)
- 100mg
- 200mg
- 300mg
- 400mg
tablet, extended release (12 hours)
- 100mg
- 200mg
- 300mg
- 450mg
tablet, extended-release (24 hours)
- 400mg
- 600mg
oral elixir
- 80mg/15mL
intravenous solution
- 400mg/250mL D5W
- 400mg/500mL D5W
- 800mg/500mL D5W