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Bioglita

Bioglita is a member of the family of medications known as thiazolidinediones. It is used to lower high blood sugar associated with type 2 diabetes. Thiazolidinediones such as Bioglita help insulin to work more effectively.

Other names for this medication:
Bioglita, Daoride, Diaglit, Diazero, Dimbest, Glime, Glimitab, Glimkap, Glito, Glitter, Gluconorm, Glucut, Glycinova, Matce, Metride, Pichromet, Piodart, Pioglaz, Pioglit, Pioglitazone, Piokap, Piolem, Piolet, Pioriv, Piosafe, Piozed, Piozol, Piozone, Piozulin, Triexer, Trigulin, Walaphage

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Also known as: Pioglitazone

Description

Bioglita is a medication that’s used to treat type 2 diabetes. This is a condition in which where your body has a high level of glucose (sugar) in your blood. Your pancreas normally makes a hormone called insulin, which takes glucose out of your blood and helps you use the sugar as a source of energy. With type 2 diabetes, your pancreas may not be making enough insulin to remove the sugar from your blood.

And if you have type 2 diabetes, your cells may also become insulin resistant. This means that your body makes insulin but isn’t responding to it by removing the sugar from your blood. So people with type 2 diabetes have high blood sugar levels.

What Bioglita does

Bioglita works by making your cells more sensitive to insulin. The goal is for your cells to take the glucose in your blood and use it more effectively as an energy source. Because you’re using your glucose more effectively, your blood glucose levels will decrease.

This lowers your risk of serious complications of type 2 diabetes, including heart disease, nerve damage such as neuropathy, and kidney failure.

How long does it take to work?

After you start using Bioglita, it may take 7 days or longer before you notice any changes in your blood glucose level. It’s important to keep taking Bioglita every day so that it can have the best chance to work in your body.

Dosage

The Bioglita dosage your doctor prescribes will depend on several factors. These include:

  • the type and severity of the condition you’re using Bioglita to treat
  • other medical conditions you may have, such as congestive heart failure (CHF)*
  • other medications that you’re taking to treat your type 2 diabetes
Typically, your doctor will start you on a low dosage. Then they’ll adjust it over time to reach the amount that’s right for you. Your doctor will ultimately prescribe the smallest dosage that provides the desired effect.

The following information describes dosages that are commonly used or recommended. However, be sure to take the dosage your doctor prescribes for you. Your doctor will determine the best dosage to fit your needs.

* <em>Bioglita</em> has a<em> boxed warning</em> for CHF. This is the most serious warning from the FDA. For more information, see “FDA warning: Congestive heart failure” at the beginning of this article.

Drug forms and strengths

Bioglita comes as a tablet that you swallow, and you’ll usually take it once a day. Bioglita is available in three strengths: 15 mg, 30 mg, and 45 mg.

Dosage for type 2 diabetes

Your doctor will likely have you start taking either a 15-mg or 30-mg dose of Bioglita once a day. If needed, they may increase the dose by 15 mg for extra control of your blood sugar. The maximum dose of Bioglita is 45 mg a day.

Your starting dose will depend on if you have other health conditions, such as CHF.* And the dose will be increased over time based on how your body responds.

And in some situations where your body may be very stressed, your doctor may need to change your dose or have you stop taking Bioglita. So tell your doctor right away if you:

  • have a fever
  • have an infection
  • have had an accident
  • have just had or will have surgery
Never change your dosage of Bioglita without first talking with your doctor. And before you start taking Bioglita, be sure to tell them about any medical conditions you have or any other medications that you take. Your doctor will determine what the best dosage is for you.

* Bioglita has a boxed warning for CHF. This is the most serious warning from the Food and Drug Administration (FDA). For more information, see “FDA warning: Congestive heart failure” at the beginning of this article.

What if I miss a dose?

If you miss your dose, wait and take Bioglita when your next dose is due. Never take two doses in 1 day. If you have questions on when to take your next dose of Bioglita after you’ve missed a dose, talk with your doctor or pharmacist.

To help make sure that you don’t miss a dose, try setting a reminder on your phone. A medication timer may be useful, too.

Will I need to use this drug long term?

Bioglita is meant to be used as a long-term treatment. If you and your doctor determine that Bioglita is safe and effective for you, you’ll likely take it long term.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. You may have signs of low blood sugar, such as extreme weakness, blurred vision, sweating, trouble speaking, tremors, stomach pain, confusion, and seizure (convulsions).

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) and away from excess moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Bioglita are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Bioglita can interact with several other medications. It’s not known to interact with supplements or foods.

Different interactions can cause different effects. For instance, some interactions can interfere with how well a drug works. Other interactions can increase the number of side effects or make them more severe.

Bioglita and other medications

Below is a list of medications that can interact with Bioglita. This list doesn’t contain all drugs that may interact with Bioglita.

Before taking Bioglita, talk with your doctor and pharmacist. Tell them about all prescription, over-the-counter, and other drugs you take. Also tell them about any vitamins, herbs, and supplements you use. Sharing this information can help you avoid potential interactions.

Bioglita and other diabetes medications

Sometimes your doctor may prescribe Bioglita along with other medications for your type 2 diabetes, such as glyburide (DiaBeta) or insulin. However, this may put you at risk for developing hypoglycemia (low blood sugar).

Hypoglycemia can cause symptoms such as dizziness, sweating, and headache. In severe cases, you may have serious complications such as a seizure or passing out.

Before starting Bioglita treatment, it’s important to tell your doctor what other medications you’re taking.

You should also talk with your doctor about what to do if you develop symptoms of hypoglycemia, especially if you’re taking multiple diabetes medications.

Bioglita and gemfibrozil

Gemfibrozil (Lopid) may interact with Bioglita. If you’re taking gemfibrozil, the level of Bioglita in your body will rise. Gemfibrozil can also increase the amount of time that Bioglita stays in your body.

If there’s too much Bioglita in your body and you’re also taking other diabetes medications such as insulin, your blood sugar can get too low. This can cause symptoms such as dizziness or sweating.

Before you start taking Bioglita, have your doctor review your all medications. They can adjust your treatment as needed.

Bioglita and rifampin

Taking rifampin (Rimactane) along with Bioglita may decrease the level of Bioglita in your body. This means that you may not get enough Bioglita, and it may not work to treat your type 2 diabetes.

If you start or stop taking rifampin while using Bioglita, your doctor may need to change your dose of Bioglita.

Bioglita and topiramate

If you take Bioglita along with topiramate (Topamax, Trokendi XR, Qudexy XR), the level of Bioglita in your body may decrease. This means that the Bioglita may not work well to treat your type 2 diabetes.

If you’re taking topiramate and Bioglita, talk with your doctor. They may recommend changing your dose of Bioglita or monitoring your blood glucose more often to be sure that Bioglita is working for you.

If you have questions about drug interactions that may affect you, ask your doctor or pharmacist.

Bioglita and herbs and supplements

There aren’t any herbs or supplements that have been specifically reported to interact with Bioglita. However, you should still check with your doctor or pharmacist before using any of these products while taking Bioglita.

Bioglita and foods

There aren’t any foods that have been specifically reported to interact with Bioglita. If you have any questions about eating certain foods with Bioglita, talk with your doctor.

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46,684 19-20 years old Swiss male conscripts and published data on 1000 Eskimos, 518 Toronto residents and 97,000 North American Adventists. Poly (ADP-ribose) synthetase (PARS) is a nuclear enzyme activated by strand breaks in DNA which are caused by reactive oxygen species (ROS) and peroxynitrite. The search for altered physiological processes in pre-eclamptic placentae requires the investigation of events at both the microvillous and basal surfaces. elegans sleep-like state with developmental changes that occur with larval moults suggests that sleep may have evolved to allow for developmental changes. Of the 17 cases of free tissue transfer using thoracoacromial vessels for anastomosis, 13 flaps were performed in 12 patients who had received double irradiation. Assessment by laboratory simulation of approaches to amelioration of peat acidification. Here we used experimental evolution with the bacterium Escherichia coli to quantify the molecular changes underlying functional innovation in 68 independent instances ranging over 22 different metabolic functions. Experiment 2 replicated this bias effect and showed that the increase in lexical decision performance due to neighbour priming is selectively due to words from a relatively sparse neighbourhood. Effects of hippocampal lesions on striatolimbic ionotropic glutamatergic receptors. The development of HRQOL instruments for children and adolescents has continued apace in recent years, particularly with regard to disease-specific questionnaires.

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Short course versus long course neoadjuvant radiotherapy remains controversial. Circadian rhythms of systolic arterial pressure (SAP) and heart rate (HR) were investigated in spontaneously hypertensive rats (SHR) and in normotensive Wistar rats (NWI) with intact SCN, grafted with SHR embryonic AH tissue containing the SCN. tuberculosis was established by the gradual depletion of nutrients in an oxygen-replete protonix 20 mg cost and controlled environment. The model describes the transient changes of fumigant concentrations in both the intergranular air and grain. Few studies have investigated the effect of hydrotherapy on the social interactions and behaviors of children with ASDs. Intra-operative hyperkalemia: a serious but under recognised complication of renal parathyroidectomy - a prospective study: how we do it.

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This study is based on current needs and what characteristics might be desirable. Protein disorder and the evolution of molecular recognition: theory, predictions and observations. Primary large cell neuroendocrine carcinomas of the skin are exceptionally rare and can be diagnosed only when a metastasis from another organ has been excluded. Synthetic chromatin approaches to probe the writing and erasing of histone modifications. We propose a robust semiparametric method to overcome the limitations of the existing methods. Understanding the impact distribution of particles entering the human respiratory system is of primary importance as it concerns not only atmospheric pollutants or dusts of various kinds but also the efficiency of aerosol therapy and drug delivery.

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A retrospective analysis of both the recipient and donor mononuclear cell suspensions supported the hypothesis that HHV-6 had been acquired from the donor with the bone marrow graft. Non-alcoholic fatty liver disease (NAFLD) is a disorder characterized by excessive fat deposits in hepatocytes without excessive alcohol intake. The programme was run by a multidisciplinary team comprising a rheumatologist, a social worker, a physical and occupational therapist, and a psychologist. In the first stage the eye velocity response is classified to obtain initial estimates of the slow phase eye velocity intervals. This process involves the ortho C-H activation of N-aryl-2-aminopyridines, and CuCl(2) was used as an oxidant.

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