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Resta 0.25 mg/500 mg Tablet

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  • Resta 0.25 mg/500 mg Tablet

Product Informations: Resta 0.25 mg/500 mg Tablet

In Insomnia Resta 0.25 mg/500 mg Tablet is a combination of two medicines that helps treat insomnia (difficulty falling or staying asleep) in people who have problems related to their sleeping habits. Insomnia may cause you to wake up earlier than usual and you may find it difficult to go back to sleep. It works by slowing down the abnormal activity of nerves in the brain to allow sleep. It also improves the sleep-wake cycle and restores it to normal. This helps you relax, feel calm and more energetic. It also helps you concentrate better and improves your quality of life.

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. Resta 0.25 mg/500 mg Tablet may be taken with or without food, but it is better to take it at a fixed time.
Resta 0.25 mg/500 mg Tablet is a combination medicine used to treat insomnia. It helps to decrease the abnormal and excessive activity of the nerve cells and calm the brain. Resta 0.25 mg/500 mg Tablet can be taken with or without food. However, it is advised to take it at the same time each day as this helps to maintain a consistent level of medicine in the body. Take this medicine in the dose and duration advised by your doctor. If you miss a dose of this medicine, take it as soon as you remember. Finish the full course of treatment even if you feel better. It is important not to stop taking this medicine suddenly without talking to the doctor. Some common side effects of this medicine include confusion, memory impairment, and depression. It may also cause dizziness and sleepiness. So, do not drive or do anything that requires mental focus until you know how this medicine affects you. It may cause weight gain or weight loss depending upon person to person. To prevent weight gain, you can eat a healthy balanced diet, avoid snacking with high-calorie food and exercise regularly. On the other hand, weight loss can be managed by increasing food portions and consulting a dietitian. If you have been taking this medicine for a long time than regular monitoring of blood and liver functions may be required. Your doctor should also know about all other medicines you are taking as many of these may make this medicine less effective or change the way it works. Inform your doctor if you are pregnant, planning pregnancy or breastfeeding.
  • Drowsiness
  • Tiredness
  • Memory impairment
  • Uncoordinated body movements
  • Depression
Alcohol : UNSAFE

It is unsafe to consume alcohol with Resta 0.25 mg/500 mg Tablet.

Pregnancy : CONSULT YOUR DOCTOR

Resta 0.25 mg/500 mg Tablet is unsafe to use during pregnancy as there is definite evidence of risk to the developing baby. However, the doctor may rarely prescribe it in some life

threatening situations if the benefits are more than the potential risks. Please consult your doctor.

Breast feeding : CONSULT YOUR DOCTOR

Resta 0.25 mg/500 mg Tablet is probably unsafe to use during breastfeeding. Limited human data suggests that the drug may pass into the breastmilk and harm the baby.

Driving : UNSAFE

Resta 0.25 mg/500 mg Tablet may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.

Kidney : SAFE IF PRESCRIBED

Resta 0.25 mg/500 mg Tablet is probably safe to use in patients with kidney disease. Limited data available suggests that dose adjustment of Resta 0.25 mg/500 mg Tablet may not be needed in these patients. Please consult your doctor.

Liver : CAUTION

Resta 0.25 mg/500 mg Tablet should be used with caution in patients with liver disease. Dose adjustment of Resta 0.25 mg/500 mg Tablet may be needed. Please consult your doctor. However, the use of Resta 0.25 mg/500 mg Tablet is not recommended in patients with severe liver disease and active liver disease.

If you miss a dose of Resta 0.25 mg/500 mg Tablet, 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.

Habit Forming::Yes|Therapeutic Class::NEURO CNS

FDC Ltd | B-8, MIDC Area, Waluj - 431 136, Dist. Aurangabad, Maharashtra


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References

FDA approved prescribing information. Levocitrizine; 1995 [revised May 2007]. [Accessed 01 Apr. 2019] (online) Available from: Read More

European Medicne Agency. Revised assessment report: Ambroxol and bromhexine containing medicinal products. 2015. [Accessed 01 Apr. 2019] (online) Available from: Read More

ScienceDirect. Ambroxol. [Accessed 01 Apr. 2019] (online) Available from: Read More

Levocitrizine. Slough, Berkshire: UCB Pharma Limited; 2007 [revised 27 Mar. 2019]. [Accessed 01 Apr. 2019] (online) Available from: Read More



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