Etizola Lite 0.25mg/5mg Tablet
Etizola Lite 0.25Mg/5Mg Tablet is usually prescribed as a sedative and a hypnotic for sleep and anxiety disorders. It is not to be used for pregnant and lactating women, for those with impaired kidney and liver functions, lung problems, and glaucoma.
There may be enhanced sedation when had with medicines like beta-blockers, antibacterials, antifungals and antipsychotics. Remember to ask the doctor any queries that you may have about the medicine and the course of the treatment.
It comes in the form of a tablet, to be taken with food. The recommended dosage for an adult is 3mg a day. Never take a double dose of Etizola Lite 0.25Mg/5Mg Tablet, it is better that you skip it till the next time you take it.
The most common side effects of Etizola Lite 0.25Mg/5Mg Tablet are drowsiness, sedation, muscle weakness and incoordination. More serious effects that urgently require medical help are fainting, slurred speech, changes in libido and tremors.
Information given here is based on the salt content of the medicine. Uses and effects of the medicine may vary from person to person. It is advisable to consult a Neurologist before using this medicine.
Use
This drug can be used in below-mentioned conditions
Insomnia
Anxiety And Nervousness
Dosage
Etizola 0.25 Tablet
Etizola 0.5 Tablet
Etizola Beta 0.25mg/20mg Tablet
Etizola Beta 0.5 Tablet
Etizola Lite 0.25mg/5mg Tablet
Etizola Plus 10 Tablet
Etizola Plus 5 Tablet
Side Effects
Here are some possible side effects of this drug
Altered Libido
Confusion
Depression
Drowsiness
Fainting
Headache
Uncoordinated Body Movements
Fatigue
Sedation
Slurred Speech
Tremor
Visual Impairment
Dosage
Are there any overdose instructions?
In case of overdose, consult your doctor.
Are there any missed dose instructions?
Missed dose should be taken as soon as possible. It is recommended to skip your missed dose, if it is the time for your next scheduled dose.
Work
As this medicine is a benzodiazepine analog, it is used for treating insomnia, anxiety and panic attacks. It primarily acts on the GABA-A receptors, preventing GABAergic transmission throughout the CNS.
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