Contraindicated in: 
- Hypersensitivity to ipratropium or any components of the product;
 - Severe/acute/deteriorating symptoms of airflow obstruction due to COPD;
 - Treatment of asthma.
 
Use Cautiously in: 
- History of seizures; 
 - Thyrotoxicosis; History of cardiovascular disorders (coronary insufficiency, arrhythmias, hypertension); 
 - Sensitivity to sympathomimetics (adrenergics); 
 - Narrow-angle glaucoma; 
 - History of bladder-neck obstruction or prostatic hypertrophy; 
 - Mild to moderate renal impairment (CCr<60 mL/min) ↑ risk of anticholinergic side effects; 
 - Severe hepatic impairment; 
 - OB: Use during pregnancy only if potential maternal benefit justifies potential fetal risk; Lactation: Use while breastfeeding only if potential maternal benefit justifies potential risk to infant; 
 - Pedi: Safety and effectiveness not established in children.
 
Exercise Extreme Caution in: 
- Concurrent use with MAO inhibitors, tricyclic antidepressants or drugs that prolong the QTc interval (↑ risk of adverse cardiovascular reactions). 
 
 
Therapeutic Classification: bronchodilators, bronchodilators
Pharmacologic Classification: beta-adrenergic agonists, anticholinergics
 
Olodaterol
Absorption: 30% absorbed following oral inhalation (from lung surface); swallowed drug in minimally absorbed.
Distribution: Extensive tissue distribution; probably enters breast milk
Metabolism/Excretion: Extensively metabolized (some by CYP3A4), only one metabolite binds to B2adrenergic receptors. Following inhalation, 57% excreted unchanged in urine, remainder in feces as drug and metabolites (84%).
Half-Life: 45 hr (following inhalation).
Tiotropium
Absorption: 19% absorbed following inhalation.
Distribution: Extensive tissue distribution; due to route of administration ↑ concentrations occur in lung.
Metabolism/Excretion: 74% excreted unchanged in urine; 25% of absorbed drug is metabolized.
Half-Life: 56 days.