Clonazepam, the active ingredient in Pase, shares common pharmacological effects with benzodiazepines, including anticonvulsants, sedatives, muscle relaxants, and anxiolytic properties. These effects result from enhanced GABAergic neurotransmission at inhibitory synapses. Benzodiazepines increase the affinity of GABA receptors for the neurotransmitter, leading to greater chloride ion flux across the postsynaptic membrane.
Studies in animals indicate that clonazepam also affects serotonin levels. Additionally, electroencephalographic (EEG) research in humans has demonstrated that clonazepam rapidly suppresses various paroxysmal activities, such as spike-and-wave discharges in the absence of seizures, slow spike waves, generalized spikes, and irregular spike patterns. Its effects are more pronounced on generalized EEG abnormalities than focal abnormalities, making it beneficial for both generalized and focal epileptic conditions.
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Pase is prescribed for the management of panic disorder, with or without agoraphobia. Panic disorder involves sudden, unexpected panic attacks along with persistent concern about experiencing further episodes or their potential consequences.
Additionally, Pase is used alone or alongside other treatments for Lennox-Gastaut Syndrome (petit mal variant), as well as akinetic and myoclonic seizures. It may also be considered for patients with absence seizures (petit mal) who have not responded to succinimides.
The long-term effectiveness of Pase beyond nine weeks has not been extensively studied in controlled clinical trials. Physicians prescribing Pase for extended periods should periodically assess its continued necessity and effectiveness.
Symptoms: Overdosing on Pase may cause drowsiness, ataxia, slurred speech, and involuntary eye movements (nystagmus). Severe overdose may lead to loss of reflexes, respiratory depression, hypotension, coma, or cardiac complications. While rarely fatal when taken alone, overdose combined with other CNS depressants (including alcohol) can be life-threatening.
Treatment:
Side Effects
Common side effects are related to central nervous system (CNS) depression. During seizure treatment, drowsiness occurs in about 50% of patients, and ataxia in around 30%, though these effects may lessen over time. Behavioral changes have been reported in approximately 25% of cases. Other possible adverse effects include:
Pase does not significantly impact the metabolism of phenytoin, carbamazepine, or phenobarbital. However, its effects on other drugs have not been fully investigated.
Pase should not be used in individuals with known hypersensitivity to benzodiazepines or those with significant liver disease. While it may be used in patients with open-angle glaucoma receiving appropriate treatment, it is contraindicated in cases of acute narrow-angle glaucoma.
Store in a dry place, away from heat and light. Keep out of reach of children.
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