Q&A: A Doctor Challenges the FDA on Safety

In May 2014, Robert P. Blankfield, MD, MS, a clinical professor of family medicine, Case Western Reserve University School of Medicine, published an editorial in an online edition of the Journal of Cardiovascular Pharmacology and Therapeutics that charged the FDA to be more vigilant about approvals of medications that can affect blood pressure, even a small amount. Dr. Blankfield, who is also a physician at University Hospitals Medical Practices, Berea, Ohio, recently spoke with MedShadow about his concerns:

MS: What prompted you to write this editorial?

I’ve been trying for a while to get some attention to this issue. Several medications that were approved by the FDA that incidentally raise blood pressure were eventually pulled from the market after reports showed that these drugs increase the risk of heart attacks and strokes. These drugs include rofecoxib (Vioxx), valdecoxib (Bextra), sibutramine (Meridia) and phenylpropanolamine.

MS: There seems to be some controversy over what constitutes a “clinically significant” increase in blood pressure. Isn’t there a standard?

The FDA has no consistent standard. Different reviewers for the FDA use different standards as to what constitutes a significant increase in blood pressure. The standards that are used are, in my opinion, too lax. The standard that the FDA ought to be using is an increase in systolic blood pressure of more 2 mm Hg, or an increase in diastolic blood pressure of more than 1 mm Hg, at least in individuals who are at high risk for cardiovascular disease. Individuals who are at high risk for cardiovascular disease include: the elderly (individuals older than age 65), individuals who already have cardiovascular disease, individuals who have diabetes and individuals who have hypertension.

Interestingly, even when a drug exceeds the unreasonably high standards used by the FDA, the FDA fails to take appropriate action. This is one aspect of the Vioxx story that has been totally overlooked by the media. For Vioxx, the blood pressure criteria that was used is that the drug had to raise the systolic blood pressure more than 20 points, and, in addition, the drug had to raise the systolic blood pressure over 140 mm Hg. Or the drug had to raise the diastolic pressure 10 points or more, and it had to raise the diastolic pressure over 90 mm Hg. Those extraordinarily large changes in blood pressure establish an extremely high threshold. Vioxx exceeded the systolic blood pressure threshold, yet the FDA failed to require the manufacturer to provide cardiovascular safety data when the drug was approved.

MS: Vioxx raised blood pressure quite high, but you seem to be saying that the FDA is ignoring smaller increases that could be significant as well.

A study published in 2002 in The Lancet, a premier medical journal, analyzed cardiovascular risk and blood pressure. The study found that there is a continuous relationship between blood pressure and cardiovascular risk. At the end of the paper, the authors write that for middle-aged adults, if the systolic blood pressure increases 2 points, then there is a 10% increase in heart attack risk and a 7% increase in stroke risk. Likewise, for a 1 millimeter increase in diastolic blood pressure, there is an identical 10% increase in heart attack risk and a 7% increase in stroke risk. It would be prudent for the FDA to incorporate that information into their review process. If the FDA did incorporate that information, then any medication that raises systolic blood pressure more than 2 mm Hg or that raises diastolic blood pressure more than 1 mm Hg should have a requirement for cardiovascular safety data, at least if the drug will be used by individuals at high risk for cardiovascular disease.

I’m saying two things: That the FDA should be paying attention to small increases in blood pressure, which it is definitely not doing.  And even when there are big increases in blood pressure that meet its criteria, in the one instance I am familiar with — Vioxx — it looked the other way.

MS: Why should we worry if these drugs are off the market now?

There are many drugs that are still on the market that modestly raise blood pressure. The following drugs all raise systolic blood pressure more than 2 mm Hg or raise diastolic blood pressure more than 1 mm Hg: duloxetine (Cymbalta), milnacipran (Ixel, Savella, Dalcipran, Toledomin), levomelnacipran (Fetzima), venlafaxine (Effexor), desvenlafaxine (Pristiq), buproprion (Wellbutrin), amphetamine salts combination (Adderall), and lisdexamfetamine (Vyvanse).

MS: Why are they out there if the others got pulled?

Although these drugs raise blood pressure, there is no cardiovascular safety data to justify regulating these drugs. The drugs that got pulled were taken off the market because safety data demonstrated an increased risk of heart attacks and strokes.

MS: Why do you think that the FDA failed to take a look at the cardiovascular risk of these drugs if they are potentially so problematic – political pressure, short staffed?

According to Norman Stockbridge, MD, PhD, Director, Division of Cardiovascular and Renal Products, FDA Center for Drug Evaluation and Research, the FDA recognizes that a modest elevation in blood pressure, even if it is undetectable in any given individual, increases the risk of heart attacks and strokes. Nonetheless, in the absence of unfavorable safety data, the FDA’s stance is that no regulatory action is indicated. Such reasoning makes sense only if the mandate of the FDA is to respond to existing data. However, it makes no sense that the FDA chooses to ignore predictable risk. The reason that there is no safety data is that the FDA failed to require such data at the time of drug approval. It is unwise policy to allow drugs that predictably increase risk to remain on the market without adequate safety data. The stance that the FDA has taken undermines its credibility as an unbiased regulatory agency.

MS: Why do you think the FDA has not responded to your editorial?

Whenever there is criticism, the FDA’s reaction seems to be to hunker down and wait for it to pass. Invariably, the storm of criticism eventually passes.

MS: How have colleagues responded to your editorial?

Several colleagues have informed me that they agree with what I am saying, including Steven Nissen, MD, Chairman of Cardiovascular Medicine at the Cleveland Clinic Foundation.

MS: If someone is on those medications, what should they do? Contact their physician?

Any reasonable physician is likely to say there is no data demonstrating an increased risk for those medications, that the risk is entirely theoretical. To which I say, shame on the FDA for not mandating the collection of the appropriate safety data. Unless there is pressure applied to the FDA to change its policies, the current situation will not change, and the problem will go on and on.


Beth Levine

Beth Levine

Beth Levine is an award-winning writer based in Stamford, CT. www.bethlevine.net


Did you find this article helpful?


Latest News

Breaking News – EpiPen Malfunction

Breaking News – EpiPen Malfunction

Just released from the FDA – Pfizer has informed the FDA that they are aware of several continuing problems that people are having using the EpiPen (epinephrine) and EpiPen Jr (epinephrine) auto-injectors and generic versions. Some of the problems are from user error and some from EpiPen malfunction. Here are…

ACE Inhibitors in the Time of Coronavirus

ACE Inhibitors in the Time of Coronavirus

Are you worried about ACE inhibitors and coronavirus? You may be hearing that one of the entry methods for the coronavirus in humans is by attaching to the ACE-2 enzyme. This has raised alarms among those with heart disease who use ACE inhibitors (with names ending in -pril, such as…

  • Advertisement