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In June 2007 during a hearing of the U.S. House of Representatives, the FDA announced that it was mandating Black Box warnings on all Actos packaging and
Diabetes drugs to get 'black box' warning. FDA to require notice of heart failure risks on labels of Avandia, Actos
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The U.S. Food and Drug Administration (FDA) recently announced that its strongest type of warning-a "Black Box" warning-will be placed on Type 2 diabetes
The FDA ordered that U.S. labeling be updated with a “black box warning” against using Actos if the patient has a history of bladder cancer.
Actos and Avandia in diabetes carry different risks of heart failure and mortality A black box warning was recently added to both drugs cautioning against their
The use of Actos, a popular diabetic drug, is associated with an increased risk of about the danger of the drug or makes a "black box warning.
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In 2009, the FDA required Actos and other drugs containing pioglitazone to carry a “black box warning” because they were associated with an
FDA has asked the makers of Actos to issue a black box warning about the serious risk of adverse cardiovascular events, such as congestive heart failure.
In 2007, the FDA added a “black box” warning to Actos's labeling, alerting doctors and patients that Actos can cause or exacerbate congestive heart failure,
Talk to an Actos injury attorney of Greg Jones Law in North Carolina about 2007 to require the manufacturer, Takeda, to put a "black box" warning on its labels.
In 2007, the FDA issued an order for a black box warning to be placed on the labels of Actos and Avandia following scientific evidence that Actos and Avandia
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Discuss Actos or Avandia use carefully with your doctor if you Black Box Warning: May cause or worsen congestive heart failure; monitor patients for signs and
The Actos Lawyers at Eichholz are here to help those who are harmed by Actos. Since then, the FDA has added a Black Box warning label to alert consumers
The FDA ordered to print a black box warning label on it. This warning label suggests that there is a link between Actos and cancer from actos.
Avandia and Actos have long been shown to increase the risk of heart The black box warning doesn't address more recent concerns that
Actos is nothing but a medicine to control the blood sugar and it is used has announced to require the black box warning to this medicine.
A new study finds Actos and Avandia heart risks similar; heart failure, stroke The study led to a black box warning of Avandia heart risks being
A Reuters report was released this past week claiming that the European Medicines Agency (EMA) is stressing new warnings that link Actos to
FDA and GlaxoSmithKline (GSK) both just announced that negotiations between the drug companies and FDA regarding the new,
Both Actos and Avandia carry a black box warning about the risk of congestive heart failure exacerbation and are contraindicated in patients with established
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So serious is the risk, Actos (pioglitazone) holds the U.S. Food and Drug Administration's tough “black box” warning, underscoring the risk of congestive heart
The risk is so serious, that the FDA instructed Takeda Pharmaceuticals to include a black box warning on Actos packaging. A black box warning
Amidst an intense debate over the safety of Type-2 diabetes drugs, the FDA has asked the makers of Actos® to issue a black box warning. A black box warning
As a result of the study conducted by Takeda Pharmaceuticals, the FDA indicated a black box warning label will be added to Actos. What is a
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The FDA has forced the manufacturer of Actos to add a black box warning regarding the drug's extremely dangerous side effects, namely the potential for heart
Black-box heart-failure warning for rosiglitazone, pioglitazone drugs for type 2 diabetes—rosiglitazone (Avandia) and pioglitazone (Actos),
NEWS UPDATE: ABC News: FDA Warns of Bladder Cancer Risk With Actos If you took In 2007, the FDA mandated a black box warning for Actos regarding its
If you have been injured by Actos, or even developed bladder cancer, then you provide a "black box warning" as well as a Medication Guide for patients that
Actos has a black box warning, stating that heart failure and liver disease patients should avoid the drug. There are numerous other side effects shown at the
The FDA's decision to request the addition of an Actos black box warning was announced during a June 2007 US House of Representatives hearing.
Actos® is currently being sold in the United States although it is now the subject This is known as a black box warning, the strongest warning
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Due to concerns as to whether Actos is safe, the FDA has asked the makers of Actos to put a “black box warning” on the Actos box, which is the
Black Box Warning For Actos and Avandia. Linda von Wartburg. Oct 31, 2007. The FDA has spoken: the heart risk warnings on labels of Avandia (rosiglitazone)
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The FDA uses black-box warnings to protect consumers, there is some William Greenlee is just one of the countless of Actos patients who feels duped.[]
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Actos is found to have the same dangerous side effects as Avandia. The FDA ordered the maker of Actos to place a black box warning alerting doctors and
In the United States, ACTOS is still being prescribed, but the FDA issued a black- box warning in 2007, which is the strongest warning that a drug can receive
The FDA has added black box warnings on Actos for cardiovascular, edema, and possible fractures. The following are some of the important Actos side effects
Black Box for Avandia and Actos: Yet another example of Pharma influence over FDA The result: a black box warning that these drugs
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Another Study Confirms Avandia, Actos Bone Fracture Risk long-awaited black box warning for Avandia’s increased risk of heart attacks.
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In 2007, the first aftermarket warning was added to the Actos® label. This warning is a black box warning, which is considered the most serious type of warning
In several instances, the FDA was even asked to place black box warnings on the Actos label by, among others, drug safety advisors, but
The FDA now requires manufacturers of Actos and its generic equivalents to place a warning on the drugâ??s packaging. This black-box warning is the
What does Actos' “black box” warning label mean? If you're taking Actos for type- 2 diabetes in Florida, you've probably been overwhelmed by warnings.
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The FDA has subsequently enforced the addition of a Black Box warning label informing consumers of the potential risk involved in taking Actos.
The U.S. Food and Drug Administration (FDA) has asked the manufacturers of Actos to issue a black box warning identifying the dangerous cardiovascular side
A black box warning (the sternest warning put on a drug label) was added to Avandia and Actos, another drug with a similar mechanism of
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In 2007, the FDA issued a "black box" warning that included both Actos and Avandia. One five-year study involving 193099 patients showed that people who
FDA Requires Actos To Have A Black Box Warning. After an intense debate over the safety of the Type-2 Diabetes drug Actos, the FDA has stated that the heart
The new black box warnings have nothing to do with heart attacks. The label will warn that the class of drugs to which both Actos and Avandia
Today, Actos carries a black box warning label, which is the most serious safety caution issued by the FDA, because the drug puts patients at a greater risk for
The federal regulator added black box warnings to Actos for bladder cancer side effects in June 2011, though it stopped short of recalling the drug pending
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The FDA announced diabetes drugs Avandia and Actos will begin carrying a ' black box' warning, the strongest level of warning issued by the
The FDA's latest Actos warning follows another high-profile warning issued in June of 2007. At that time, the agency issued a "black box
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Actos Bladder Cancer Lawsuit resources and information. In 2007 the FDA required Takeda to include a "black box" warning the highest level of warning on
The commissioner of the Food and Drug Administration yesterday informed a hearing of the House Committee on Oversight and Government
However, Actos has not been recalled in America. The FDA required that Actos have a black box warning on its label. The black box warning is
It was especially designed to determine whether an Actos might increase the The agency even placed a black box warning on the label to
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Avandia and Actos were approved by the U.S. Food and Drug The FDA added a "black box" warning to the class of drugs in 2007, noting that
Diabetes drugs to carry heart failure cautions. Makers of Avandia and Actos have agreed to add 'black-box' warning
The black box warnings have to do with the well-known propensity of Then I was switched after another 1 1/2 months to Actos and within 2
The diabetes patients taking Actos for more than 12 months are situating themselves in bladder cancer. The FDA issued a BlackBox warning
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If you have been affected by the diabetes medication Actos, please contact our and Eli Lilly Pharmaceuticals) include a black box warning on every package.
Actos is in the same class of diabetic drugs as Avandia and in 2007 the FDA determined that the labels for these drugs should contain a black box warning
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In June of 2011, before the study was even complete, the FDA had enough evidence to order that Actos carry a Black-Box warning, the strongest warning that a
if actos has a " black box warning" i would not take it.my doctor told me to still take it and i refused.. then she prescribed metformin and
FDA has asked makers of Actos to put black box warning. Actos connected with bladder cancer and congestive heart failure.
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FDA seeks Avandia, Actos 'Black Box' warning. During the June 2007 congressional hearing into the Food and Drug Administration's (FDA's) approval process
In June of 2007, the FDA issued a "black box warning" due to reports of liver and heart problems among patients taking Actos and Avandia.
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The Actos side effects above, have been included in stringent warnings from the FDA and resulted in what is known as a Black Box warning for the drug.
In 2007, amidst an intense debate over the safety of Type-2 diabetes drugs, the FDA asked the makers of Actos to issue a black box warning
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The FDA ordered a black box warning label placed on all boxes of Actos, warning of the increased risk of baldder cancer. Bladder cancer is a particularly serious
Learn about safety information and FDA warnings for Actos, a type-2 diabetes drug linked to increased risk of bladder cancer and heart failure.
There is a “black box warning” for Actos. The statement that Actos “may be associated with an increased risk of bladder cancer.” was added to the “Warnings and
The FDA said the class of diabetes drugs that includes Avandia and Actos will carry the agency's toughest black box warning that the drugs are
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In the United States Actos is still being prescribed however the FDA did issue a " black box" warning for the drug in 2007. A black box warning label is the
A “black box” warning was added to Avandia in the United States in Actos ( pioglitazone) was introduced as a treatment option for type 2
Both Avandia and Actos are used to treat Type-2 Diabetes, both have been The FDA has given Avandia a black box warning, a warning that
Black-Box Heart-Failure Warning for Rosiglitazone, Pioglitazone drugs for type 2 diabetes-- rosiglitazone (Avandia) and pioglitazone (Actos),
Actos, manufactured in Osaka, Japan by Takeda Pharmaceuticals,
Since 2007, the FDA required Avandia to include a black box warning for patients The other is a 3-year comparison of Avandia and Actos, based on more than
As a result, the FDA required the producers of Actos to release and now include a black box warning (highest and strongest label change)
Actos FDA Warning. Bladder cancer affects more than 52000 men and 17000 women each year in the United States. This form of cancer occurs when abnormal
Actos is still on the market in the U.S.; however, the FDA has demanded that a Black Box Warning about the possible increased risk of bladder cancer be added
So far, the FDA has not issued a black box warning for Actos. However, some experts expect to see Actos follow a similar path as Avandia in terms of restrictions.
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Where Eli Lilly's negligence comes in,is their KNOWING and not informing consumers (black box warning) until the FDA demanded it. Lilly's incentive not to
Actos was linked to bladder cancer. A Dallos Actos attorney discusses why the drug is still being sold in the U.S. after being banned in France and Germany.
As of this week, it's become clear critics and activists have won their point. The FDA has announced Avandia and Actos will soon bear a
The drug now bears a black box warning about exactly this risk. by comparing the patient records of elderly patients using Avandia and alternative drug Actos,
The U.S. and Canada have not suspended the sales of Actos as of yet but have required Takeda to put a black box warning label on the drug
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Another four diabetes drugs from the same class, including Actos, will also carry a similar black-box message, which is the agency's strongest label warning.
In September 2007, a 'black box' warning was added to Actos packaging due to the concern over congestive heart failure (similar to the warning with Avandia).
No ,the FDA has not officially recalled Actos yet. They did require Actos to print a " BLACK BOX" warning on its label . Despite the FDA's warning about the link
Rather, the FDA has increased the drug's black box warnings and called for further studies. Yet, the evidence connecting Actos and bladder
Avandia, Actos, Avandamet and Avandaryl received black box warnings about increased risks of congestive heart failure in August of 2007,
Taking Actos can increase the risk of bladder cancer. A black box warning is the strongest FDA-requested label change that can be added to a drug.
A black box warning in the medication guide states before you begin to take Actos®, you should tell your doctor if you have ever had congestive heart failure,
The FDA disclosed Wednesday during a Congressional hearing it has asked GlaxoSmithKline and Takeda Pharmaceutical to add a "black box"
The FDA has asked the makers of Actos to issue a black box warning about the serious risk of adverse cardiovascular events, including heart
For now, the FDA review of Actos is continuing, together with a request for a warning—presumably a black box warning—with regard to the risk
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For some, Actos causes water retention and that situation has a black box warning on this medications. Because Actos lowers insulin resistace it make the
Risks associated with Avandia are not unique. The FDA also required a black box warning on Actos in 2007, alerting patients that the drug may
The FDA requested that the makers of Actos® issue a black box warning containing a list of issues regarding health safety. This type of warning is one of the
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Companies Will Include Boxed Warning on Drug Label. The U.S. This class includes Avandia (rosiglitazone), Actos (pioglitazone) Avandaryl
Black Box Warning For Actos and Avandia. The FDA has spoken: the heart risk warnings on labels of Avandia (rosiglitazone) and Actos (pioglitazone) will now
The FDA has acknowledged the very real risks of taking Actos and now requires the company to issue a black box warning on the medication's
Increased risk of suffering Actos congestive heart failure became such a widely known problem that the FDA had to step in and issue a “black box” warning - the
However, Actos's packaging carries its own “black box” warning, the FDA's most serious alert, stating that, in some patients, “Thiazolidinediones
The Actos package insert and bladder cancer warnings (PDF) in the the bladder cancer information within an Actos “black box” warning,
FDA Alert Against Taking Actos. The FDA announced during Congressional hearings that it has decided to issue “black box” warnings about cardiac risks with
Although the FDA had mandated a black box warning for Actos regarding possible heart failure risks in 2007, the warnings became even more stringent this past
Actos® has a black box warning, for its increased risk of heart attack. However, new studies are linking the drug to an increased risk of developing bladder
Takeda Pharmaceuticals will now have to add language to the warning label or “ black box” label of Actos stating that long term use of the drug
Actos entire monograph, dosing, interactions, and patient education at Epocrates Online, the leading provider of drug and disease Black Box Warnings .
Actos Lawsuit News - FREE Case Evaluation : Learn If You Qualify For In addition to the black box warning, the FDA has issued a public
The FDA issued a warning in June 2011, after a five-year study of the makers of Actos and a similar drug, Avandia, to place a "black box" alert
And although Actos appears to have lower cardiovascular risks than like Avandia — Actos carries an FDA-required black box warning on its
The FDA has since enforced the addition of a Black Box warning label to inform consumers of the potential risk involved in taking Actos. At Jonathan Perkins
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The FDA has mandated that the manufacturers of the drug now issue a black box warning regarding other side effects of Actos® as well.
Go beyond basic drug info with this in-depth overview on Actos for diabetes, including discussions on its black box warning, clinical research, side effects and
Actos, like Avandia, is a class of medication called thiazolidinedione (TZD). These drugs What Does it Take to Get a Black Box Warning?
In May 2007, the Food and Drug Administration asked Takeda Pharmaceuticals to add a “black-box” warning to its diabetes drug Actos after it was linked to an
In 2007, the FDA required a black-box warning for all pioglitazone hydrochloride medications, including Actos, alerting the public to the possibility that the drug
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The FDA also requires ACTOS to have a “black box warning.” A black box warning is a warning that appears on the packaging inserts for prescription drugs that
My Doctor haqd me on both Avandia & Actos. Once I was aware of the black box warning on these meds I took myself off these meds.
In August 2007, after a number of reports, the FDA decided that the official Actos ® drug information must include a black-box warning concerning the risk of
A black box warning is the severe FDA-asked label modification that can be cumulated to a drug. Present Status Of Actos Adverse Effects. The FDA is presently
The FDA says that the diabetes drug, Actos, may increase the risk of bladder needs to be a black box warning - the most stringent available to the FDA - or if
Actos Side Effects Prompt Black-Box Warning. Actos sales spiked as many type-2 diabetics stopped taking Avandia because it caused some patients to develop
12/10/2008- The widely prescribed diabetes drugs Avandia and Actos have .. The Black Box warning is the most severe warning a drug can have, and this is
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In August 2007, the FDA issued a black-box warning concerning Actos after the drug was linked to an increased risk of heart failure. Other studies have also
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The request from FDA for a black box warning for the labels of Avandia and Actos involved only increased risk for heart failure associated with
Black box warning from actos. January 21, 2012 | Author. Nowadays people take lot of medicines without the consultation of doctor. It is very harmful to intake
The Actos suspension is effective July 11, 2011”. The United States Food and Drug Administration (FDA) ordered a black box warning that the
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The ad stated, “Actos lower[s] blood sugar without increasing your risk of Even after the class-wide FDA black box warning for congestive
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Actos is available in 15 mg, 30 mg and 45 mg pills. Actos side effects are generally few in patients who have no congestive heart failure, but because of the
In fact, the heart-failure risk is so great that Actos, as well as related drugs such as Avandia (rosiglitazone), have a black-box warning from the
On June 11, 2007 the FDA requested a black box warning label for both Actos and Avandia, another Type 2 diabetes medication, due to the increased risk of
The FDA issued a black box warning label for Actos in June of 2007 during a House of Representatives hearing. During this hearing the fact that the FDA was
The FDA's latest Actos warning follows another warning issued in June of 2007. At that time, the agency issued a "black box warning" requiring
Actos Receives a Black Box Warning Label. As a result of the study conducted by Takeda Pharmaceuticals, the FDA indicated a black box
The drugs affected by the FDA Black Box Warning are as follows: Avandia® ( rosiglitazone maleate) Tablets; Actos® (pioglitazone hydrochloride) Tablets
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Many people with Type 2 Diabetes are taking Actos® to control their action and required the manufacturer to issue a black box warning, the
Actos currently carries a "black box" warning regarding the potential for the drug to cause or worsen congestive heart failure, a serious condition which prevents
The bladder cancer risk finding prompted the FDA to add a warning to the medication label known as a “black box warning”. If you are taking Actos and
Health officials announced this week that the diabetes drugs Avandia and Actos will contain "black box" warnings. "Black box" warnings are the
Avandia® and Actos®: Type 2 Diabetes Drugs The special warnings, also called "Black Box” Warnings, advise doctors and Type 2 diabetes
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The FDA has since enforced the addition of a Black Box warning label informing consumers of the potential risk involved in taking Actos. Similar studies have
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June 16, 2011—The FDA warned Actos patients that long-term use of the drug A black box warning is the strongest warning available to the FDA to inform
In fact, the FDA has given Actos a “black box” warning; the strongest possible warning the FDA can give before this drug is taken off the market
Later, scientific studies determined that Actos could also cause cardiovascular events and fractures. FDA then required a Black Box warning for
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If you are taking the drug Actos in place of Avandia, click here for important Since November 2007, Avandia's label has included a black box warning.
In June 2007 the FDA required the manufacturers of Actos and a similar-acting drug, Avandia, to add a "black box" warning to the drugs'
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Blackbox warning. A separate research project over five years and using almost 200000 patients showed that the risk of developing bladder cancer could rise by
Avandia and Actos are both drugs for treating type 2 (adult onset) diabetes. Avandia is A black box warning is the strongest FDA warning.
FDA to Require Black Box Warning on Avandia, Actos. The U.S. Food and Drug Administration (FDA) recently announced in congressional testimony that it
In 2007, amidst an intense debate over the safety of Type-2 diabetes drugs, the FDA asked the makers of Actos to issue a black box warning about the serious
Black Box Warning for Actos. The FDA has issued a Safety Alert and ordered that warnings be added to the labels of all medications containing Pioglitazone.
But there is no black box warning on Actos, and a number of studies have suggested that the same safety issues do not apply. There are a
Black box warnings indicate that the drug in question has been linked to hoping to prove that Avandia had better therapeutic outcomes than Actos, an diabetic
In 2007, the FDA ordered Takeda Pharmaceuticals, the manufacturer of Actos, to include a black-box warning on its product. The warning explained that Actos
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Learn about Actos heart risks, including risk of congestive heart failure, from The FDA requires the drug's packaging to carry a black box warning due to the
So far, there is no black box concerning Actos bladder cancer on the label. The FDA stated in its June 2011 warning that it will continue to
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Actos carries a black box warning for exacerbation or cause of congestive heart failure. Patients who experience congestive heart failure because of Actos may
A black box warning of the danger of congestive heart failure that may be exacerbated or caused by Actos® was added to the drug's label in August 2007.
Actos New Black Box Warning - More severe than the first one Takeda. Takeda's Actos to include black box heart warning 25th June 2007
Actos is still being prescribed throughout the United States - even since it's "black box" warning was issued in 2007 by the FDA including Actos and Avandia.
Don't Read Those Black-Box Drug Label Warnings, They Will Make Two drugs, Avandia (rosiglitazone) and Actos (pioglitazone) serve as an
Discuss type 2 diabetes and living with type 2 diabetes. Huge site dedicated to discussing diabetes. Manage diabetes by discussing it with
Actos- it has a black box warning. get off the crap. i came close to congestive heart failure w/ it. short of breath even at rest. fish oil- take Krill Oil
Recently, there has been new evidence and research that shows a connection between Actos use and bladder cancer. Based on this research that shows a link
The FDA has asked the makers of Actos® to issue a black box warning on a variety of health safety issues. A black box warning can be among the strongest
TZD diabetes drugs to get black box warning. tzd, diabetes, drugs, get, Avandia (rosiglitazone) and Takeda's Actos (pioglitazone), as well as
Makers of Certain Diabetes Drugs Agree to 'Black Box' Warning of Heart Actos, Avandaryl, Avandamet, and Duetact -- will get the black box
Call an experienced New York Actos bladder cancer lawsuit attorney at Rosenbaum & Rosenbaum in New York City at What is a black box warning? The FDA
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Actos pioglitazone benefit and risk, side effects of this medication used for blood Pharmaceutical Company Ltd., have agreed to add the "black-box" warnings.
The FDA may require drug companies to include a black box warning if it Accutane; Actos; Avandia; Avastin; Baycol; Bextra; Celebrex; Crestor; DePuy Hip
For additional details regarding speak with an Actos Injury Lawyer. Notice: The FDA doesn't give a stronger warning than the black box
Actos is no stranger to FDA black box warnings. In 2007, a black box warning was issued saying that Actos may cause heart failure.
Although the FDA has required a “black box” warning on Actos since 2007 for its potential to cause or exacerbate congestive heart failure, only recently did the
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Actos, which is a Type-2 diabetes drugs, now has a FDA black box warning about the serious risk of adverse cardiovascular events, including heart attack, heart
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What is a black box warning for Actos? No Comments. If you suffer from bladder cancer after taking Type 2 diabetes drug Actos, you may know
Actos drug and side effects information provided by experienced Actos attorneys. Learn more A black box is the strongest warning that the FDA mandates.
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Last week Actos received a “black box warning” from the U.S. Food and Drug Administration, the agency's strongest level of caution. Actos, and
Although the FDA has required a black box warning for Actos, it remains on the market to this day. If you or someone you love has experienced adverse side
Posted in Actos | Tagged Black box warning, Bladder cancer, Diabetes Care, Diabetes mellitus type 2, Food and Drug Administration, Heart
The FDA announced that Actos and Avandia will receive black box warnings about the increased risk of heart failure. This warning does not
Is Actos Safe? France Says "No". In 2007, the FDA required a black-box warning on Actos alerting the public to its potential to cause or worsen congestive heart
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FDA has asked the makers of Actos to issue a black box warning about the serious risk of adverse cardiovascular events, such as congestive
3. Pioglitzone, sold under the brand name Actos. . Also the FDA Black Box Warning included both Actos, ACTOplus met and Duetact, as can be seen below.
Metformin/glucophage ? I take the actos plus met and januvia. anyone ever heard anything Avandia will have the black box warning. I bet Actos is next. :( .
Rosiglitazone (Avandia) and pioglitazone (Actos) already carry black box warnings for seniors with heart trouble. Nov. 24, 2008
“Even after the class-wide FDA black box warning for congestive heart failure was added in 2007, pioglitazone [Actos] use was largely
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First approved by the FDA in 1999, Actos initially raised suspicion when the FDA required the medication to have a black box warning, because of increased risk
Researchers found that the use of Avandia and Actos was far more The FDA added a “black box” warning in 2007 regarding the risk of heart
The FDA considers the risk to be so serious that in 2007 the ordered that the manufacturer to place what is known as a "blackbox" warning on the Actos package,
Actos carries FDA black box warnings about the risk of congestive heart failure in patients. It has also been linked to stroke, hypertension, and worsening heart
Heart disease is also associated with the health risks of taking Actos. The FDA decided to issue a black box warning for the adverse cardiovascular occurrences
In 2007, the FDA received sufficient data from clinical studies to issue a black box warning for Actos, stating congestive heart failure as one of
In August, the FDA posted a black box warning of the link to bladder cancer on Actos Labels. Thousands of Actos injury lawsuits were filed.
We are filing lawsuits on behalf of diabetes patients who have taken Actos. The "black-box warning" is the strongest warning label the FDA can issue with
In 2007 the FDA required a black-box warnings on the package insert, or label, of Avandia and Actos labels which states that these diabetes drugs should not be
These Actos side effects have been included in stringent warnings from the FDA and resulted in what is known as a Black Box warning for the drug. For those
Later reports of congestive heart failure among those taking Actos resulted in the FDA issuing a black box warning (the most severe warning)
The U.S. Food and Drug Administration (FDA) has announced that a black box warning has been placed on the popular diabetes drugs Avandia and Actos
On June 15th, the FDA warned consumers and doctors about the potential bladder cancer risk linked to Actos. It formally updated labels and added black box
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