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Disopan 2 Tablet prevents your brain from producing the chemicals that cause anxiety, therefore alleviating the symptoms of excessive anxiety and concern. It can also help with the symptoms of Generalised Anxiety Disorder such as restlessness, weariness, difficulty focusing, irritability, and sleep issues. As a result, the Disopan 2 Tablet will make your everyday tasks easier and more productive. Even if you feel OK, keep taking this medication. Stopping abruptly can lead to major difficulties.
You are recommended not to consume alcohol along with Disopan 2 to avoid unpleasant side effects like drowsiness, dizziness, or sleepiness.
Disopan 2 Tablet 50's belongs to pregnancy Category D. It is usually not recommended during pregnancy. However, consult your doctor if you are pregnant or planning for pregnant.
Avoid breastfeeding while on treatment with Disopan 2 Tablet '50s.
Disopan 2 Tablet may cause dizziness, drowsiness, and visual disturbances which may affect the ability to drive or operate machinery. So, do not drive or operate heavy machinery if you feel sleepy or dizzy after taking Disopan 2 Tablet 50s.
Disopan 2 is to be taken with caution, especially if you have a history of kidney disorders. The dose may have to be adjusted by your doctor.
Disopan 2 is to be taken with caution, especially if you have a history of Liver diseases/conditions. The dose may have to be adjusted by your doctor.
Take this medicine in the dose and duration as advised by your doctor. Swallow it as a whole. Do not chew, crush or break it. Disopan 2 may be taken with or without food, but it is better to take it at a fixed time.
Disopan 2 is a benzodiazepine. It works by increasing the action of a chemical messenger (GABA) which suppresses the abnormal and excessive activity of the nerve cells in the brain.
If you miss a dose of Disopan 2, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular schedule. Do not double the dose.
A prescription drug called Disopan 2 is used to treat panic and anxiety disorders, as well as epilepsy (seizures). It helps to calm the brain and lessen abnormal and excessive nerve cell activity.
Clonazepam has pharmacological properties similar to those of benzodiazepines, including anticonvulsant, sedative, muscle relaxing, and anxiolytic effects. An increase in GABAergic neurotransmission at inhibitory synapses mediates the effects of benzodiazepines on the central nervous system. The presence of benzodiazepines increases the positive allosteric modulation of the GABA receptor for the neurotransmitter, which causes released GABA to have a greater impact on the postsynaptic transmembrane chloride ion flow.
There is more proof that clonazepam affects serotonin in animals. According to animal studies and electroencephalographic studies in humans, clonazepam suppresses a wide variety of paroxysmal activity, including spike and wave discharge in the absence of seizures (petit mal), slow spike-wave, generalized spike-wave, spikes with temporal or other locations, as well as irregular spikes and waves. More frequently than abnormalities in particular areas, general EEG abnormalities are repressed. These studies suggest that clonazepam may be useful in both generalized and localized epilepsies.
Oral:
Adults:
Pediatric Patients:
The initial dose for infants and children (up to 30 kg of body weight or 10 years of age) should be between 0.01 and 0.03 mg/kg/day but not more than 0.05 mg/kg/day given in two or three divided doses to reduce drowsiness.
Phenytoin, carbamazepine, and phenobarbital pharmacokinetics do not appear to be affected by clonazepam. Clonazepam's impact on the metabolism of other medications has not been studied.
It should not be used in individuals who have a history of benzodiazepine hypersensitivity, as well as those who have clinical or biochemical indications of severe liver damage. It can be utilized in individuals with open-angle glaucoma who are on the right medication, but it's not recommended for acute narrow-angle glaucoma.
Pregnancy:
It cannot be ruled out from preclinical studies that clonazepam has the possibility of birth defects. From epidemiological evaluation, there is evidence that anticonvulsants can be used as teratogens. However, it is difficult to determine from published epidemiological reports which drug or drug combination is the cause of neonatal defects. There is also the possibility that other factors exist. For example, genetic factors or epilepsy itself may be more important than medications in causing birth defects. In these cases, the drug should be used for pregnant women only when the potential benefits outweigh the risks to the fetus. During pregnancy, clonazepam should only be used if there are compelling indications. The use of high doses in the last trimester of pregnancy or during delivery can cause irregular heartbeats in the fetus and neonatal hypothermia, hypotonia, mild respiratory depression, and poor diet. It should be remembered that both pregnancy itself and sudden withdrawal from the drug can cause seizures. Benzodiazepines occasionally cause withdrawal symptoms in newborns.
Nursing Mothers:
Although only a small amount of the active ingredient in clonazepam has been found to pass into breast milk, mothers receiving this drug should not breastfeed. If there are convincing indications for clonazepam, breastfeeding should be stopped.
Keep away from light and heat in a dry area. Keep out of children's reach.
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