Generic Name: Generic actos
What is Generic Actos?
The decision whether to continue the patient on therapy with ACTOS should be guided by clinical judgment pending laboratory evaluations. If jaundice is observed, drug therapy should be discontinued.
Therapy with ACTOS should not be initiated if the patient exhibits clinical evidence of active liver disease or the ALT levels exceed 2. Patients with mildly elevated liver enzymes ALT levels at 1 to 2. Initiation or continuation of therapy with ACTOS in patients with mildly elevated liver enzymes should proceed with caution and include appropriate clinical follow-up which may include more frequent liver enzyme monitoring.
If ALT levels exceed 3 times the upper limit of normal, the test should be repeated as soon as possible. Macular Edema: Macular edema has been reported in post-marketing experience in diabetic patients who were taking pioglitazone or another thiazolidinedione.
Some patients presented with blurred vision or decreased visual acuity, but some patients appear to have been diagnosed on routine ophthalmologic examination. Patients with diabetes should have regular eye exams by an ophthalmologist, per the Standards of Care of the American Diabetes Association.
Additionally, any diabetic who reports any kind of visual symptom should be promptly referred to an ophthalmologist, regardless of the patient's underlying medications or other physical findings see ADVERSE REACTIONS. This difference was noted after the first year of treatment and remained during the course of the study.
If you are about to be started on any new medicine, remind your doctor and pharmacist that you are taking ACTOS. If you are going to have surgery, tell the surgeon or anaesthetist that you are taking this medicine.
It may affect other medicines used during surgery. If you are about to have any blood tests, tell your doctor that you are taking this medicine. It may interfere with the results of some tests. Keep all of your doctor's appointments so that your progress can be checked. Your doctor may do some tests from time to time to make sure the medicine is working and to prevent unwanted side effects.
If you stop taking it suddenly, your condition may worsen or you may have unwanted side effects. ACTOS alone is unlikely to affect your ability to drive or operate machinery. However, be careful whilst driving or operating machinery if using ACTOS combination with other diabetes medicines.
If your blood glucose level becomes too low, you may feel dizzy, lightheaded, weak or tired and your reaction time may be slower than usual. If you have any of these symptoms, do not drive or do anything else that could be dangerous. Tell your doctor or pharmacist as soon as possible if you experience any undesirable effect or feel unwell while you are taking ACTOS.
This medicine helps most people with type 2 diabetes not controlled by diet, but it may have unwanted side effects in some people. All medicines can have side effects.
How should I take Generic Actos?
Clinical Studies Monotherapy Three randomized, double-blind, placebo-controlled trials with durations from 16 to 26 weeks were conducted to evaluate the use of ACTOS as monotherapy in patients with type 2 diabetes. Figure 1 shows the time course for changes in HbA1c in this 26-week study. Add-on to Sulfonylurea Trials Two clinical trials were conducted with ACTOS in combination with a sulfonylurea. Add-on to Insulin Trials Two clinical trials were conducted with ACTOS in combination with insulin.
What is the most important information I should know about ACTOS. ACTOS can cause serious side effects, including new or worse heart failure.
What should I avoid while taking Generic Actos?
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Generic Actos side effects
In 2011, the FDA issued a warning that Actos may increase the risk of bladder cancer if it is used for over a year. However, it remains available in the United States. If you experienced serious side effects after taking Actos or another defective drug, you should consult the product liability attorneys at Moll Law Group.
We represent claimants nationwide, and billions of dollars have been recovered in cases in which we have been involved. Thousands of Actos product liability and wrongful death lawsuits are pending in the U. In one lawsuit, the plaintiff alleged that the manufacturer purposely destroyed several hard drives related to Actos and bladder cancer that would have damaged the manufacturer.
In the spring of 2015, the manufacturer and its subsidiary reached an agreement that is expected to resolve most pending litigation.
Common Generic Actos ide effects may include:
Learn about life as a diabetic.
It is not known if ACTOS will harm your unborn baby.
You may report side effects to FDA at 1-800-FDA-1088.
If you notice other effects not listed above, contact your doctor or pharmacist.
The drug has already been pulled from the market in Germany, France and India. In 2011, the FDA issued a warning to patients using Actos and later updated the Warning and Precautions section of the label to include additional risk information they required a bladder cancer warning be placed on the Actos label and insert. Plaintiffs state that Takeda concealed the Actos bladder cancer risk from them and they are actively pursuing justice for being wronged.
Where can I get more information?
Both women declined to comment afterward.
Although they have been shown to rarely cause liver damage, the FDA requires that liver tests be done before treatment start, every two months for the first year and periodically thereafter.