Classes
DEA Class; Rx
Common Brand Names; Klonopin
- Antianxiety Agents;
- Anxiolytics, Benzodiazepines;
- Anticonvulsants, Benzodiazepine
Description
Oral long-acting benzodiazepine with no active metabolites
Approved for panic disorder in adults and as prophylaxis of absence, petit mal variant (Lennox-Gastaut syndrome), akinetic, and myoclonic seizures in adult and pediatric patients
Avoid coadministration with opioids if possible due to potential for profound sedation, respiratory depression, coma, and death
Indications
Indicated for the alternative treatment of absence seizures, petit mal variant (Lennox-Gastaut syndrome), and akinetic and myoclonic seizures (myoclonia).
Contraindications
Significant hepatic impairment
Documented hypersensitivity
Acute narrow angle glaucoma
Adverse Effects
- Somnolence (37%)
- Abnormal coordination (5-10%)
- Ataxia (5-10%)
- Depression (5-10%)
- Dizziness (5-10%)
- Fatigue (5-10%)
- Memory impairment (5-10%)
- Upper respiratory infection (5-10%)
- Confusion (1-5%)
- Dysarthria (1-5%)
- Rhinitis (1-5%)
- Coughing (1-5%)
- Urinary frequency (1-5%)
- Impotence (1-5%)
- Decreased libido (1-5%)
- Increased salivation
- Worsening tonic-clonic seizures
Warnings
Withdraw gradually when used for panic disorder
Use caution in COPD, sleep apnea, renal/hepatic disease, open-angle glaucoma (questionable), depression, suicidal ideation
Not recommended in patients with depressed neuroses, psychotic reactions, severe respiratory depression, myasthenia gravis (allowable in limited circumstances), acute alcohol intoxication
Anterograde amnesia reported benzodiazepine use
May cause CNS depression and impairs ability to perform hazardous tasks
Hyperactive or aggressive behavior reported with benzodiazepines in pediatric/adolescent patients and in psychiatric patients
Increased risk of suicidal thoughts/behavior reported with antiepileptic agents; monitor patient for suicidal behavior and notify health-care provider immediately
Use with caution in patients with a history of drug abuse or acute alcoholism; drug dependency possible; prolonged use may result in psychological and physical dependence
Use with caution in patients with compromised respiratory function
May have porphyrogenic effect; use with caution in patients with porphyria
Not for concomitant administration with alcohol or other CNS-depressant drugs
When used in patients in whom several different types of seizure disorders coexist, clonazepam may increase incidence or precipitate onset of generalized tonic-clonic seizures (grand mal); may require addition of appropriate anticonvulsants or increase in dosages; concomitant use of valproic acid and clonazepam may produce absence status
Pregnancy and Lactation
There are no adequate and well-controlled studies of Klonopin in pregnant women; available human data on risk of teratogenicity are inconclusive; there is insufficient evidence in humans to assess effect of benzodiazepine exposure during pregnancy on neurodevelopment
Effects on breastfed infant and on milk production are unknown; developmental and health benefits of breastfeeding should be considered along with mother’s clinical need for therapy and any potential adverse effects on breastfed infant from drug or from underlying maternal condition
Maximum Dosage
20 mg/day PO.
20 mg/day PO.
Weight more than 30 kg: 20 mg/day PO for seizures; safety and efficacy have not been established for panic disorder.
Weight 30 kg or less: 0.1 to 0.2 mg/kg/day PO for seizures; safety and efficacy have not been established for panic disorder.
0.1 to 0.2 mg/kg/day PO for seizures; safe and effective use not established for panic disorder.
0.1 to 0.2 mg/kg/day PO for seizures.
Safety and efficacy have not been established.
How supplied
Clonazepam
tablet dispersible: Schedule IV
- 0.125mg
- 0.25mg
- 0.5mg
- 1mg
- 2mg
tablet: Schedule IV
- 0.5mg
- 1mg
- 2mg