Salagen
pilocarpine (oral)†
(pye-loe-kar-peen) pilocarpine,Salagen
(trade name)Classification
Therapeutic: none assignedPharmacologic: cholinergics
†For ophthalmic use of pilocarpine, see
Indications
Action
- Increased sweating, gastric secretions,
- Increased bronchial secretions,
- Increased tone and motility of the urinary tract, gallbladder, and biliary duct smooth muscle.
Therapeutic effects
Pharmacokinetics
Time/action profile
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
PO | 20 min | 1 hr | 3–5 hr |
Contraindications/Precautions
Adverse Reactions/Side Effects
Central nervous system
- dizziness
- headache
- weakness
Ear, Eye, Nose, Throat
- amblyopia
- epistaxis
- rhinitis
Cardiovascular
- edema
- hypertension
- tachycardia
Gastrointestinal
- nausea (most frequent)
- vomiting (most frequent)
- dyspepsia
- dysphagia
Genitourinary
- urinary frequency
Dermatologic
- flushing (most frequent)
- sweating (most frequent)
Neurologic
- tremors
Miscellaneous
- chills
- voice change
Interactions
Drug-Drug interaction
Concurrent use of anticholinergics will ↓ the effectiveness of pilocarpine.Concurrent use of bethanechol or ophthalmiccholinergics may result in ↑ cholinergic effects.Concurrent use with beta blockers may ↑ the risk of adverse cardiovascular reactions (conduction disturbances).Route/Dosage
Head and Neck Cancer PatientsAvailability
Nursing implications
Nursing assessment
- Assess oral mucosa for dryness and ulceration periodically during therapy.
Potential Nursing Diagnoses
Impairedoral mucous membrane (Indications)Implementation
- Do not confuse Salagen (pilocarpine) with selegiline.
- Oral: Use lowest dose that is tolerated and effective for maintenance.
Patient/Family Teaching
- Instruct patient to take medication as directed.
- Caution patient that pilocarpine may cause visual changes, especially at night; avoid driving or other activities requiring alertness until effects of medication are known.
- Advise patient to drink adequate daily fluids (1500–2000 mL/day), especially if sweating occurs. Less than adequate fluid intake may lead to dehydration.
Evaluation/Desired Outcomes
- Increased salivary gland secretion in patients with xerostomia.
- Decrease in dry mouth in patients with Sjögren’s syndrome. Full effects in cancer patients may not be seen for up to 12 wk or 6 wk in patients with Sjögren’s syndrome.