Cymbalta: Yet Another Neuropathy Drug With Dangerous Side Effects

Today's post from enjuris.com (see link below) is one you should not take lightly if your doctor has prescribed Cymbalta (duloxetine) for your neuropathy symptoms. Like most drugs used to treat nerve damage symptoms, it was originally prescribed for another purpose (in this case, depression and related problems). Then because of the way it works on the brain receptor cells, it was assumed that it will help with nerve pain. However, because the potential side effects (especially pertaining to withdrawal) are so powerful, for many patients it has proved to cause greater problems than the neuropathy itself. Now neuropathy patients are mostly well aware that they're being used as guinea pigs for a whole range of drugs - this happens when you have an incurable condition - but doctors are obliged to warn them of potential side effects and they frequently don't. The consequences of taking Cymbalta can be so serious as to be life-threatening, so serious discussions must first take place before taking it. Unfortunately, most patients blindly believe their doctors (who in their turn, blindly believe the pharmaceutical company's sales pitch) because that's how we were raised. Those days are changing and need to change, so patients need to take more responsibility for the drugs they take, by doing as much research as they can and questioning any prescription until they are satisfied it's safe. It's a fact of life and we need to change our attitudes to protect ourselves against unwanted side effects. Cymbalta is by no means the only neuropathy drug with side effects worse than the nerve pain itself - there's a long list...so I understand that you'll take anything to reduce the impact of neuropathy symptoms (we're only human) but please do the research, question your doctors and get assurances before taking anything that was originally designed for another disease.
 

Cymbalta Withdrawal Symptoms and Side Effects
Written by: Enjuris Editors

 

Health problems not on the box’s label

Cymbalta is a popular medication primarily used to treat depression; it is also used for many “off-label” conditions like chronic pain and nerve issues. One might assume a doctor would be clear with all of the potential side effects, as well as what happens when you cease taking the drug, the Cymbalta withdrawal symptoms. Perhaps the box would be clearer, in any case? Not so. Find out how many patients were put on a medication with no intention of ever removing them from it.

Cymbalta has been embroiled in controversy for years. That is most likely because of withdrawal symptoms, collectively labeled as Cymbalta Discontinuation Syndrome. That sounds ominous, doesn’t it?

Who uses Cymbalta?

Cymbalta, also known by its generic version of duloxetine, is intended to treat major depressive disorder and general anxiety disorder. It is in a class of medications called SSNRIs (selective serotonin and norepinephrine reuptake inhibitors). These affect brain chemicals in ways meant to control depression and anxiety, though sometimes they themselves cause the very problems they’re supposed to be treating.

Do you use Cymbalta or duloxetine for chronic pain or fibromyalgia? You should read this. Tweet this

After a time on the market, duloxetine was approved for the off-label treatment of conditions like fibromyalgia, diabetic neuropathy, and chronic muscle and joint pain.


How does Cymbalta work?

Put simply, Cymbalta is believed to block the reuptake of serotonin and norepinephrine within the central nervous system (CNS). When the number of pro-inflammatory cytokines increases, depressive tendencies are thought to worsen. Duloxetine allegedly reduces pro-inflammatory cytokines while raising anti-inflammatory cytokines. (We say “allegedly” because there are no scientific studies to confirm this.)

Enjuris tip: Not sure if your Cymbalta is causing problems? Think you may be experiencing Cymbalta withdrawal symptoms? Speak with your doctor first and eliminate other possibilities before pursuing a legal claim.

It does, however, treat pain because of its analgesic qualities. That treats conditions like fibromyalgia and chronic pain.

A brief history of Cymbalta and related medical issues

Duloxetine was created by Eli Lilly researchers in 1986 and patented in 1990. Eli Lilly attempted to present it to the Food and Drug Administration in 2001, though the FDA stated the product was unapprovable in its current state because of manufacturing and control standpoint violations in their Indianapolis facility. They also noted concerns about potential drug-caused liver damage (hepatotoxicity). Eli Lilly fixed the problems at the Indianapolis outpost, and with a liver damage warning printed on the prescription information, the drug was approved by the FDA in 2004.

Many patients feel electrical “brain zaps” as a withdrawal symptom when stopping Cymbalta. This was not listed as a side effect. Tweet this

Duloxetine was approved for the use of stress urinary incontinence – but only in the United Kingdom. Eli Lilly decided not to pursue this effort in the United States because the FDA would not grant approval based on what was submitted (despite the fact it was approved for this use in 38 foreign markets).

Side effects

There is a long list of side effects on Cymbalta’s label. Many of them were not known about when the drug was first prescribed, and only after patients’ complained louder and louder did authorities investigate.

Adverse effects include:

Dry mouth
Nausea
Heavy sweating
Dizziness
Diarrhea
Vomiting
Heartburn

Headaches
Muscle cramps
Drowsiness
Weakness
Less or no appetite
Trouble urinating
Sexual dysfunction

The most unexpected and unwanted side effect, however, came from the cessation of the drug. When patients tried to end their regimens, they found themselves unable to do so, facing concerning withdrawal symptoms.

Cymbalta Discontinuation Syndrome

No medication label talked about the electric-like shocks patients experienced when they tried to stop taking duloxetine. They even have a name: “brain zaps.” These painful sensations are followed by confusion, dizziness and agitation.

It is recommended that patients stop taking duloxetine over a gradual period rather than an abrupt cessation. Cymbalta withdrawal symptoms and side effects from weaning too quickly are:

Irritability
Nausea
Vomiting
Anxiety
Dizziness
Diarrhea

Nightmares
Sweating
Vertigo
Fatigue
Headaches
Peripheral neuropathy in the hands and feet

Patients claim that these adverse effects were not made clear prior to beginning duloxetine regimens.

Some people even need to be hospitalized because of discontinuation syndrome. It was not until 2009 that the Food and Drug Administration conceded the fact that Cymbalta’s label was insufficient compared to its risks. It also carries the black box warning because of the suicide risk.

Existing litigation for Cymbalta

Patients were certified as a class-action lawsuit in 2012. They claimed that Eli Lilly had misrepresented Cymbalta, and consumers from Missouri, Massachusetts, California and New York petitioned to be certified as a class in 2013. (Before allowing a class-action suit to proceed, the various plaintiffs must be certified by the court.) However, in 2017, after several legal struggles and false starts, the appellate court dismissed the plaintiffs’ claim.

Cymbalta withdrawal can cause anything from vomiting to mood swings to peripheral neuropathy. Tweet this

The one multidistrict litigation (MDL) for Cymbalta litigation was denied by the federal district court in 2014 when 28 individual cases attempted to consolidate. Another attempt was made with 40 cases in 2015. As of 2018, Eli Lilly is in settlement talks with 140 pending Cymbalta lawsuits. So far, the manufacturer has won four individual plaintiffs.

Most notable was how the company reported only 1% of users experiencing discontinuation symptoms, while plaintiffs claim that number is between 44% to 50%.

According to the National Pain Report,

As early as 2005, research indicated a high rate of what medical professionals call “adverse events” when patients stopped taking Cymbalta. This Lilly study found that 44 percent of patients involved in several short-term trials had “adverse events” when they suddenly stopped taking duloxetine (the generic name for Cymbalta). The most common withdrawal symptoms cited were dizziness, nausea, headache, paresthesia (tingling/numbness, usually in the limbs), vomiting, irritability and nightmares. About 10 percent of these patients had “severe” withdrawal symptoms. A longer and larger Lilly trial involving 1,279 patients found that 50 percent of patients experienced withdrawal symptoms.

FDA actions regarding Cymbalta

The FDA has moved slowly to address the dangers associated with Cymbalta. While the suicide of a teenage boy on Christmas Eve prompted them to add the strictest of warnings, the black box, which indicates the medication causes suicidal thoughts and behaviors.

They added other warnings as well:
Liver disease (2005)
Misleading ads (2005)
Urinary retention warning (2008)
Withdrawal symptoms (2009)
Advisory committee review (2010)
Blood pressure warning (2014)
Serotonin Syndrome (2017)
Takotsubo Cardiomyopathy, AKA Broken Heart Syndrome (2017) 

What to do if Cymbalta causes issues

Your first step should be to speak with your doctor to rule out other health issues. Your second step should be to talk with a lawyer. Remember, each state has a different statute of limitations (AKA the time window in which to file your legal claim). Some states only offer one year to file a personal injury case, so do this sooner rather than later. An attorney can preserve your claim.

Do keep in mind that pharmaceutical cases take a long time to finish. It could be a decade before you see any type of real compensation.

For a case as complicated as this, you must get a lawyer with years of experience and who knows how to work with other attorneys. Consider looking through the Enjuris directory for someone in your state who can join your team.

https://www.enjuris.com/pharmaceutical-liability/cymbalta.html