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Topiramate- patient information

Topiramate 

Overview 


The most well-known use of topiramate is as an anticonvulsant—a drug used to treat epilepsy. When patients are given Topiramate, it may cause some uncertainty for them and their family without a prior seizure history. The U.S. Food and Drug Administration initially authorized Topiramate   for the therapy for epilepsy and, most lately, for migraine headache prevention. Its labeled usage refers to authorized indications. However, in clinical settings, doctors often prescribe medication when published clinical research, case reports, or their own clinical trials are used for unlabeled (“off-label”) applications. 
Experiences bolster the medicines’ safety and effectiveness. Using Topiramate   to treat bipolar disorder It is usage off-label for disorder, especially in cases of extreme mania, is an example. Additional circumstances in which Topiramate   is often used off-label include alcohol and cocaine, as well as eating problems (such as binge eating and bulimia) retreat.

According to preliminary clinical research, Topiramate   could work well when combined with another medication.  Manic and depressed stages of bipolar illness are treated with a mood stabilizer. The benefit of Topiramate   over certain other mood stabilizers, including Depakote, is that it doesn’t cause weight gain or may result in a little reduction in weight. Topiramate   may offset the negative effect when taken in combination with treatment of another mood stabilizer’s weight gain and provide both mood stabilization and mood management.


Information about Dosing 


The recommended starting dose of Topiramate   is often between 12.5 and 25 mg per day, with weekly dosage increases of 25 mg. The typical age range for dosages used to stabilize mood is 100–200 mg/day, split into smaller doses. Dosage ought not to surpass the standard daily limit of 400 mg.


Typical Side Effects 


Topiramate   side effects that are most often reported are sleepiness, exhaustion, poor coordination, and gastrointestinal symptoms, ataxia (difficulty walking), problems paying attention and focusing, such as cramping in the abdomen, nausea, and vomiting. These adverse effects are often more common and strong at greater concentrations.

Adverse Events and Safety Measures 


Topiramate   might make you sleepy and less attentive, particularly in the beginning of your treatment. Patients need to take care When operating a vehicle or carrying out activities requiring attentiveness.


Kidney Stones 


Kidney stones occurred in 1.5% of individuals receiving Topiramate   treatment. Kidney stone risk became apparent to be greater in males receiving Topiramate   treatment. By consuming more fluids to encourage the production of pee, the risk of kidney creation of kidney stones might be reduced.

Central Nervous System 


Topiramate   side effects linked to the central nervous system include mental and physical slowness, difficulty concentration problems, unbalance or dizziness, disorientation, and impatience. Elderly people might be especially susceptible to falling and losing their equilibrium.

 


Acidosis Metabolic 


Topiramate   has the potential to produce metabolic acidosis, an electrolyte imbalance. This negative response is uncommon in most cases, but those with chronic diarrhea, severe respiratory conditions, kidney problems, or sensitivity may be higher in certain medical situations. Among the clinical indicators of metabolic acidosis include quick breathing when at rest, general symptoms including fatigue and appetite loss, and a fast heartbeat.

Any of these symptoms should be reported by patients to their doctor.
Metabolic acidosis diagnosis may be aided by a test in the lab to gauge the blood bicarbonate level.
 


Utilization during pregnancy and nursing: Category C

 
Insufficient controlled research has been conducted on Topiramate   in pregnant women to assess the medication’s potential danger to the fetus and the mother. However, given that Topiramate   has been linked to some concerns, there may be dangers for people due to Fetal deformities in experiments on animals. When pregnant, Topiramate   usage should be avoided at all costs particularly during the first trimester. The patient may keep taking Topiramate   if they relapse and pose a higher risk to the mother and fetus. alternative medicine or therapy may be used, or you may choose to take it after providing the doctor with informed permission.

If Topiramate   is eliminated from human breast milk is unknown. But breastfeeding moms shouldn’t take Topiramate. Breastfeeding should not begin or should be discontinued if there is no other option.

 


Potential Interactions with Drugs 


When Topiramate   is used with other drugs, it may change how they are metabolized and affect the amounts of these drugs. Lowering the levels may lessen the medication’s efficacy; on the other hand, The individual may become more vulnerable to the harmful effects of the medicine when levels are raised. Additional physicians’ researches may also have an impact on Topiramate   blood levels. 

  • Alcohol consumption should be avoided by patients on Topiramate   since it may worsen sedation and fatigue. Additionally, alcohol’s sedative properties may have a depressive impact, masking its therapeutic benefits of Topiramate   and making therapy more difficult.
  •  Oral contraceptive estrogens When oral medication is used with Topiramate, estrogen-containing contraceptives, the quantity of Reduced estrogen levels might lessen the effectiveness of the birth control method and perhaps the outcome resulting in an unexpected pregnancy.  
  • carbamazepine concentrations may be notably lower than Topiramate   Significantly, when used with Tegretol, it reduces the efficacy of Topiramate.  
  • Topiramate   and (phenytoin) concentrations may be much lower Significantly, when combined with Dilantin, it lowers the efficacy of Topiramate.  
  • Acetazolamide, or Diamox, and other carbonic anti-anhydrase agents, Topiramate   combined with known drugs as inhibitors of carbonic anhydrase, like Diamox, may make kidney stones more likely, hence one should be kept away from.  

 

overindulgence

 
An overdose on Topiramate   might be dangerous, depending on how much is used. symptoms that are not life-threatening symptoms of an overdose include headache, somnolence, ataxia (reduced coordination while walking), and dizziness. In extreme circumstances, an overdose may cause delirium, renal and hepatic failure, and coma.

Treating any suspected overdose as an emergency is imperative. The individual has to be brought to the emergency space for care and observation. The prescription drug container (as well as any other medication suspected in the overdose) need to be brought up as well, as the details on the medication label may be useful in helping the treating physician figure out how many tablets the patient has taken.

Precaution Points to Remember 


  • If you forget to take a dosage, catch up by taking it two to three hours later than planned. If it’s near, Skip the missed dosage and resume your usual dosing regimen for the next scheduled dose. Never take double doses.
    • To lessen gastrointestinal distress, use Topiramate   right away after meals or during eating.
    • Keep up a sufficient fluid intake, particularly if you are pregnant, to reduce the chance of kidney stones developing prone to kidney stones.
  • Topiramate   may make you drowsy and sedentary, particularly when starting treatment, and it may also make you less attentive When driving or doing other duties that call for attentiveness, proceed with care.
  • Keep the medicine out of direct sunlight and dampness, in the light-resistant container that came with it. Warmth and moisture may hasten the disintegration of your drug, causing it to lose its medicinal consequences.
    • Make sure kids can’t get to your medicine.

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